Oncolytic viruses for modified mhc expression

ABSTRACT

The present disclosure provides for recombinant oncolytic viruses with gene deletions or insertions which result in downregulation of Major Histocompatibility Complex class I and alternatively or additively upregulation of Major Histocompatibility Complex class II. Immunologic and pharmaceutical compositions comprising these recombinant viruses and methods of using these compositions are also presented.

CROSS REFERENCE

This application is a continuation of U.S. Application No. 18/080,253,filed Dec. 13, 2022, which is a continuation of PCT/US2022/026703 filedApr. 28, 2022, which claims the benefit of priority to U.S. ProvisionalApplication No. 63/182,243 filed Apr. 30, 2021, each of which isincorporated by reference herein in its entirety.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has beensubmitted electronically in ASCII format and is hereby incorporated byreference in its entirety. Said ASCII copy, created on May 24, 2023, isnamed 199249_716302_SL.XML and is 69,632 bytes in size.

BACKGROUND

Cancer is the second leading cause of death in the United States.Challenges for commercially available therapies exists around selectivetargeting of cancer cells, localized gene expression, and reaching andmodifying the tumor microenvironment (TME). Thus, there remains a needfor improved compositions and methods of use to address thesechallenges.

BRIEF SUMMARY

Provided herein are compositions, wherein the composition comprises: anoncolytic virus, wherein the oncolytic virus comprises a genomemodification, wherein the genome modification comprises an exogenousnucleic acid encoding for an MHC I inhibitor. Further provided hereinare compositions, wherein the genome modification further comprises: adeletion or functional deletion of an endogenous nucleic acid encodingan MHC II inhibitor; or an exogenous nucleic acid that results inactivation or enhanced activation of MHC II presentation. Furtherprovided herein are compositions, wherein the genome modificationfurther comprises: a deletion or functional deletion of an endogenousnucleic acid encoding an MHC II inhibitor; and an exogenous nucleic acidthat results in activation or enhanced activation of MHC IIpresentation. Further provided herein are compositions, wherein thedeletion or functional deletion of the endogenous nucleic acid encodingthe MHC II inhibitor comprises a deletion or functional deletion of avaccinia virus gene encoding protein A35. Further provided herein arecompositions, wherein the deletion or functional deletion of thevaccinia virus gene encoding protein A35 is a deletion or functionaldeletion of gene WR158. Further provided herein are compositions,wherein the exogenous nucleic acid that results in activation orenhanced activation of the MHC II presentation encodes for a proteinselected from: an apoptosis inhibitor protein; a necrotic cell deathactivator protein; an autophagy enhancer protein; an asparaginylendopeptidase; a class II transactivator; an interferon-gamma; aToll-like receptor activator; or a dendritic cell maturation activator.Further provided herein are compositions, wherein the exogenous nucleicacid encodes for the autophagy enhancer protein, and wherein theautophagy enhancer protein is HMGB1 or a functional domain or a variantthereof. Further provided herein are compositions, wherein the exogenousnucleic acid encodes for the dendritic cell maturation activator,wherein the dendritic cell maturation activator comprises osteopontin,TNF-alpha, or a functional fragment or variant thereof. Further providedherein are compositions, wherein the protein encoded by the exogenousnucleic acid is fused to a secretion sequence, a cell permeabilizingdomain, or a combination thereof. Further provided herein arecompositions, wherein the oncolytic virus is a poxvirus, an adenoassociated virus, an adenovirus, Newcastle disease virus (NDV), Reovirus(RV), mengovirus, Myxoma virus (MYXV), Measles virus (MV), HerpesSimplex virus (HSV), Vaccinia virus (VV), Vesicular Stomatitis virus(VSV), and Polio virus (PV). Further provided herein are compositions,wherein the poxvirus comprises a betaentomopoxvirus, a yatapoxvirus, acervidpoxvirus, a gammaentomopoxvirus, a leporipoxvirus, a suipoxvirus,a molluscipoxvirus, a crocodylidpoxvirus, an alphaentomopoxvirus, acapripoxvirus, an avipoxvirus, or a parapoxvirus. Further providedherein are compositions, wherein the poxvirus is a vaccinia virus.Further provided herein are compositions, wherein the MHC I inhibitorcauses an inhibition or partial inhibition of MHC I presentation.Further provided herein are compositions, wherein the exogenous nucleicacid encoding the MHC I inhibitor comprises a gene encoding one or morecowpox virus proteins. Further provided herein are compositions, whereinthe exogenous nucleic acid encoding the MHC I inhibitor comprises a geneencoding cowpox protein CPXV012 or a functional fragment or a variantthereof. Further provided herein are compositions, wherein the exogenousnucleic acid encoding the MHC I inhibitor comprises a gene encodingcowpox protein CPXV203 or a functional fragment or a variant thereof.Further provided herein are compositions, wherein the exogenous nucleicacid encoding the MHC I inhibitor comprises a gene encoding at least oneof: Epstein-Barr virus encoded nuclear antigen 1 protein; Herpes simplexvirus encoded ICP47 protein; Herpes simplex virus encoded UL49.5protein; Cytomegalovirus encoded US6, US2, US3, US11, or gp48 protein;Epstein-Barr Virus encoded BNLF2a protein; Adenovirus encoded E3-19Kprotein; Human Immunodeficiency Virus or Simian Immunodeficiency Virusencoded Nef protein; Kaposi’s sarcoma-associated herpesvirus encodedkK3, vIRF3 or kK5 protein; or a dominant negative form of IRF7 or IRF3.Further provided herein are compositions, wherein the MHC I inhibitorcomprises a TAP inhibitor. Further provided herein are compositions,wherein the TAP inhibitor acts wholly or primarily within infectedcells. Further provided herein are compositions, wherein the genomemodification reduces an immune response targeting a virus-infected tumorcell and increases an immune response targeting cells surrounding thevirus-infected tumor cell. Further provided herein are compositions,further comprising a deletion of a thymidine kinase gene. Furtherprovided herein are compositions, further comprising an exogenousnucleic acid encoding a hyaluronidase. Further provided herein arecompositions, wherein the hyaluronidase is PH-20 or HysA. Furtherprovided herein are compositions, wherein the oncolytic virus is avaccinia virus, and the vaccinia virus is a Western Reserve strainVaccinia virus (ATCC VR-1354), a Copenhagen strain, an IHD strain, aWyeth strain (ATCC VR-325), a NYCBOH strain, a Tian Tan strain, a Listerstrain, an Ankara strain (ATCC VR-1508 or ATTC VR1566), a USSR strain,or an ACAM2000 strain.

Provided herein are compositions, wherein the composition comprises anoncolytic virus, wherein the oncolytic virus comprises a genomemodification; wherein the genome modification comprises a deletion orfunctional deletion of a vaccinia virus gene encoding A35 protein andinsertion of an exogenous gene encoding a cowpox protein CPXV012 or acowpox protein CPXV203. Further provided herein are compositions,wherein the oncolytic virus is a poxvirus, an adeno associated virus, anadenovirus, Newcastle disease virus (NDV), Reovirus (RV), mengovirus,Myxoma virus (MYXV), Measles virus (MV), Herpes Simplex virus (HSV),Vaccinia virus (VV), Vesicular Stomatitis virus (VSV), and Polio virus(PV). Further provided herein are compositions, wherein the poxviruscomprises a betaentomopoxvirus, a yatapoxvirus, a cervidpoxvirus, agammaentomopoxvirus, a leporipoxvirus, a suipoxvirus, amolluscipoxvirus, a crocodylidpoxvirus, an alphaentomopoxvirus, acapripoxvirus, an avipoxvirus, or a parapoxvirus. Further providedherein are compositions, wherein the oncolytic virus is a vacciniavirus. Further provided herein are compositions, wherein the exogenousgene encoding cowpox protein CPXV012 is at a locus of the gene encodingA35 protein of a vaccinia virus. Further provided herein arecompositions, wherein the exogenous gene encoding cowpox protein CPXV203is at a locus of the gene encoding A35 protein of a vaccinia virus.Further provided herein are compositions, wherein the genomemodification further comprises at least one of: an exogenous nucleicacid that codes for a chemokine receptor or a functional domain or avariant thereof; or an exogenous nucleic acid that codes for a cytokineor a functional domain or a variant thereof. Further provided herein arecompositions, comprising the exogenous nucleic acid that codes for acytokine or a functional domain or a variant thereof, wherein thecytokine comprises at least one of: interleukin-2 (IL-2),interleukin-15/ interleukin-15Ra (IL15/IL15Ra), interleukin-7 (IL-7), ora functional domain or a variant thereof. Further provided herein arecompositions, wherein the genome modification comprises an insertion ofan exogenous nucleic acid that codes for a fusion protein comprising acytokine and a metabolic modulator protein. Further provided herein arecompositions, comprising the exogenous nucleic acid that codes for thechemokine receptor or a functional domain or a variant thereof, whereinthe chemokine receptor comprises at least one of: CXCR4, CCR2, orfunctional domains or variants thereof. Further provided herein arecompositions, wherein the chemokine receptor comprises the CXCR4 or afunctional domain or a variant thereof. Further provided herein arecompositions, wherein the chemokine receptor comprises the CCR2 or afunctional domain or a variant thereof, wherein the CCR2 comprises awild-type CCR2 or a mutated CCR2. Further provided herein arecompositions, wherein the exogenous nucleic acid that codes for thechemokine receptor or a functional domain or a variant thereof comprisesa codon optimized sequence. Further provided herein are compositions,wherein the exogenous nucleic acid that codes for the chemokine receptoror a functional domain or a variant thereof comprises a non-codonoptimized sequence. Further provided herein are compositions, whereinthe genome modification comprises mutation or a complete or a partialdeletion of a viral gene comprising at least one of: A52R, B15R, K7R,A46R, N1L, E3L, K1L, M2L, C16, N2R, B8R, B18R, or VH1 of a vacciniavirus or a functional domain or fragment or variant thereof, or anycombinations thereof. Further provided herein are compositions, furthercomprising a deletion of a thymidine kinase gene. Further providedherein are compositions, further comprising an exogenous nucleic acidencoding a hyaluronidase. Further provided herein are compositions,wherein the hyaluronidase is PH-20 or HysA. Further provided herein arecompositions, wherein the oncolytic virus is a vaccinia virus, and thevaccinia virus is a Western Reserve strain Vaccinia virus (ATCCVR-1354), a Copenhagen strain, an IHD strain, a Wyeth strain (ATCCVR-325), a NYCBOH strain, a Tian Tan strain, a Lister strain, an Ankarastrain (ATCC VR-1508 or ATTC VR1566), a USSR strain, or an ACAM2000strain.

Provided herein are pharmaceutical compositions comprising thecomposition according as described herein and a pharmaceuticallyacceptable excipient. Further provided herein are pharmaceuticalcompositions, wherein the excipient comprises one or more of a bufferingagent, a stabilizer, an antioxidant, a binder, a diluent, a dispersingagent, a rate controlling agent, a lubricant, a glidant, a disintegrant,a plasticizer, a preservative, or any combinations thereof. Furtherprovided herein are pharmaceutical compositions, wherein the excipientcomprises disodium hydrogen phosphate dihydrate, sodium dihydrogenphosphate dihydrate, sodium chloride, myo-inositol, sorbitol, or anycombinations thereof. Further provided herein are pharmaceuticalcompositions, wherein the pharmaceutical composition does not comprise apreservative. Further provided herein are pharmaceutical compositions,further comprising one or more of a preservative, a diluent, and acarrier. Further provided herein are pharmaceutical compositions,further comprising an additional active ingredient or a salt thereof.Further provided herein are pharmaceutical compositions, wherein theexcipient is sterile water. Further provided herein are pharmaceuticalcompositions, further comprising an additional active ingredient,wherein the additional active ingredient is an anti-cancer agent or afurther oncolytic virus.

Provided herein are methods of reducing growth of a cancer cell, themethods comprising administering to a cancer cell: the composition orthe pharmaceutical composition as described herein.

Provided herein are methods for treating cancer, the method comprising:administering to a subject having a cancer, the composition or thepharmaceutical composition as described herein. Further provided hereinare methods, wherein the administering comprises an intratumoraladministration, an intraperitoneal administration, an oraladministration, an intravenous administration, an intranasaladministration, a sublingual administration, a rectal administration, atransdermal administration, or any combination thereof. Further providedherein are methods, comprising administering a further therapy, whereinthe further therapy comprises chemotherapy, radiation, oncolytic viraltherapy with an additional virus, treatment with immunomodulatoryproteins, a CAR T cellular therapy, an anti-cancer agent, or anycombinations thereof. Further provided herein are methods, wherein thefurther therapy comprises administering an immunomodulatory agentcomprising anti-CD33 antibody and variable region thereof, an anti-CD11bantibody and variable region thereof, a COX2 inhibitor, a cytokine, achemokine, an anti-CTLA4 antibody or an antigen binding fragmentthereof, an anti-PD-1 antibody or an antigen binding fragment thereof,an anti-PD-L1 antibody or an antigen binding fragment thereof, or a TLRagonist.

Provided herein are methods of treatment comprising administering to asubject in need thereof the composition or the pharmaceuticalcomposition as described herein. Further provided herein are methods,wherein the administering comprises an intratumoral administration.Further provided herein are methods, wherein the administering comprisesa systemic administration. Further provided herein are methods, whereinthe systemic administration comprises at least one of: anintraperitoneal administration, an oral administration, an intravenousadministration, an intranasal administration, a sublingualadministration, a rectal administration, a transdermal administration,or any combination thereof. Further provided herein are methods, whereinthe subject has a cancer, and wherein the cancer is at least one of: amelanoma, a hepatocellular carcinoma, a breast cancer, a lung cancer, anon-small lung cancer, a peritoneal cancer, a prostate cancer, a bladdercancer, an ovarian cancer, a leukemia, a lymphoma, a renal cellcarcinoma, a pancreatic cancer, an epithelial carcinoma, a gastric/ GEjunction adenocarcinoma, a cervical cancer, a colon carcinoma, acolorectal cancer, a duodenal cancer, a pancreatic adenocarcinoma, anadenoid cystic, a sarcoma, a mesothelioma, a glioblastoma multiforme, aastrocytoma, a multiple myeloma, a prostate carcinoma, a hepatocellularcarcinoma, a cholangiocarcinoma, a pancreatic adenocarcinoma, a head andneck squamous cell carcinoma, a cervical squamous-cell carcinoma, anosteosarcoma, an epithelial ovarian carcinoma, an acute lymphoblasticlymphoma, a myeloproliferative neoplasm, or any combination thereof.Further provided herein are methods, wherein the composition or thepharmaceutical composition is administered at a dosage from about 10⁶PFU/mL to about 10¹⁰ PFU/mL of the oncolytic virus. Further providedherein are methods, wherein the composition or the pharmaceuticalcomposition is administered at a dosage of about 3 × 10⁹ PFU/mL of theoncolytic virus. Further provided herein are methods, wherein thecomposition or the pharmaceutical composition is administered in threedoses, and wherein each of the three doses is administered in an amountand period of administration independent of any other dose. Furtherprovided herein are methods, wherein the three doses are administered ata first dose, a second dose, and a third dose, and, wherein the firstdose is lower than the second dose, and the second dose is lower thanthe third dose. Further provided herein are methods, wherein the threedoses are administered at a first dose, a second dose, and a third dose,and wherein the first dose is higher than the second dose, and thesecond dose is higher than the third dose. Further provided herein aremethods, wherein the period of administration for the three doses iseach, independently, about 1 day, about 2 days, about 3 days, about 4days, about 5 days, about 6 days, about 1 week, about 2 week, about 3weeks, about 4 weeks, about 6 weeks, about 7 weeks, about 8 weeks, about9 weeks, about 10, weeks, about 12 weeks, about 4 months, about 5months, about 6 months, about 7 months, about 8 months, about 9 months,about 10 months, about 11 months or about 1 year. Further providedherein are methods, wherein the composition or the pharmaceuticalcomposition independently comprises a liquid dosage form that isadministered at a volume from about 1 mL to about 5 mL, about 5 mL to 10mL, about 15 mL to about 20 mL, about 25 mL to about 30 mL, about 30 mLto about 50 mL, about 50 mL to about 100 mL, about 100 mL to 150 mL,about 150 mL to about 200 mL, about 200 mL to about 250 mL, about 250 mLto about 300 mL, about 300 mL to about 350 mL, about 350 mL to about 400mL, about 400 mL to about 450 mL, about 450 mL to 500 mL, about 500 mLto 750 mL, or about 750 mL to 1000 mL. Further provided herein aremethods, wherein the composition or the pharmaceutical composition isadministered in a liquid dosage form, a solid dosage form, an inhalabledosage form, an intranasal dosage form, a liposomal formulation, adosage form comprising nanoparticles, a dosage form comprisingmicroparticles, a polymeric dosage form, or any combination thereof.Further provided herein are methods, wherein the composition or thepharmaceutical composition is administered for a duration of about 1day, about 2 days, about 3 days, about 4 days, about 5 days, about 6days, about 1 week, about 2 week, about 3 weeks, about 4 weeks, about 6weeks, about 7 weeks, about 8 weeks, about 9 weeks, about 10, weeks,about 12 weeks, about 4 months, about 5 months, about 6 months, about 7months, about 8 months, about 9 months, about 10 months, about 11months, or about 1 year. Further provided herein are methods, whereinthe composition or the pharmaceutical composition is administered oncedaily, twice daily, once every week, once every two weeks, or once everythree weeks. Further provided herein are methods, wherein thecomposition or the pharmaceutical composition is administered as a bolusinjection or a slow infusion. Further provided herein are methods,wherein the administration of the composition or the pharmaceuticalcomposition results in a first peak viral load after about 1 hour toabout 3 days and a second peak viral load after about 3 days to about 10days from administration of a first dose. Further provided herein aremethods, comprising administration of a further therapy, wherein thefurther therapy is administered for a duration of about 1 day, about 2days, about 3 days, about 4 days, about 5 days, about 6 days, about 1week, about 2 week, about 3 weeks, about 4 weeks, about 6 weeks, about 7weeks, about 8 weeks, about 9 weeks, about 10, weeks, or about 12 weeks.Further provided herein are methods, wherein the further therapy isadministered once daily, twice daily, once every 1 day, once every 2days, once every 3 days, once every 4 days, once every 5 days, onceevery 6 days, once every 1 week, once every 2 week, once every 3 weeks,once every 4 weeks, once every 6 weeks, once every 7 weeks, once every 8weeks, once every 9 weeks, once every 10, weeks, once every 12 weeks,once every 4 months, once every 5 months, once every 6 months, onceevery 7 months, once every 8 months, once every 9 months, once every 10months, once every 11 months, or once every 1 year. Further providedherein are methods, wherein the further therapy is administered in aliquid dosage form, a solid dosage form, an inhalable dosage form, anintranasal dosage form, a liposomal formulation, a dosage formcomprising nanoparticles, a dosage form comprising microparticles, apolymeric dosage form, or any combination thereof. Further providedherein are methods, wherein the further therapy is administered orally,intravenously, by an intratumoral injection, by intraperitonealinjection, or by radiation. Further provided herein are methods, whereinthe further therapy comprises chemotherapy, radiation, oncolytic viraltherapy with an additional virus, treatment with immunomodulatoryproteins, a CAR T cellular therapy, an anti-cancer agent, or anycombinations thereof. Further provided herein are methods, wherein thefurther therapy comprises administration of an immunomodulatory agentcomprising anti-CD33 antibody and variable region thereof, an anti-CD11bantibody and variable region thereof, a COX2 inhibitor, a cytokine, achemokine, an anti-CTLA4 antibody or an antigen binding fragmentthereof, an anti-PD-1 antibody or an antigen binding fragment thereof,an anti-PD-L1 antibody or an antigen binding fragment thereof, or a TLRagonist. Further provided herein are methods, wherein the furthertherapy comprises administration of the anti-cancer agent, wherein theanti-cancer agent is a chemotherapeutic agent. Further provided hereinare methods, wherein the subject is human.

Other objects, features and advantages of the present invention willbecome apparent from the following detailed description. It should beunderstood, however, that the detailed description and the specificexamples, while indicating preferred embodiments of the invention, aregiven by way of illustration only, since various changes andmodifications within the spirit and scope of the invention will becomeapparent to those skilled in the art from this detailed description.

BRIEF DESCRIPTION OF THE DRAWINGS

The novel features of the disclosure are set forth with particularity inthe appended claims. A better understanding of the features andadvantages of this disclosure will be obtained by reference to thefollowing detailed description that sets forth illustrative embodiments,in which the principles of this disclosure are utilized.

FIG. 1 depicts the change in B16 tumor volume, shown in cubicmillimeters on the y-axis, following treatment with vehicle formulatedbuffer (VFB), or recombinant vaccinia virus comprising: a TK deletion(HCCTKM); TK and A52R deletions and substitution of the gene encodingthe A35 protein with a cowpox CPXV012 gene (WO0434N); or TK and A52Rdeletions without insertion of the exogenous nucleic acid (WO416N).

FIGS. 2A and 2B depict the change in Renca (FIG. 2A) or EMT6 (FIG. 2B)tumor volume, shown in cubic millimeters on the y-axis, followingtreatment with vehicle formulated buffer (VFB), or recombinant vacciniavirus comprising: (1) a TK gene deletion and insertion of nucleic acidencoding the cowpox virus V012 protein; (2) a WR158 gene deletion andinsertion of nucleic acid encoding the cowpox virus V012 protein; (3) aTK gene deletion and insertion of nucleic acid encoding dominantnegative interferon regulatory factor 7 (dnIRF7); or (4) a TK genedeletion and insertion of nucleic acid encoding viral interferonregulator factor 3 (vIRF3).

DETAILED DESCRIPTION OF THE DISCLOSURE

While preferred embodiments of this disclosure have been shown anddescribed herein, it will be obvious to those skilled in the art thatsuch embodiments are provided by way of example only. Numerousvariations, changes, and substitutions will now occur to those skilledin the art without departing from this disclosure. It should beunderstood that various alternatives to the embodiments of thisdisclosure described herein may be employed in practicing thedisclosure.

This disclosure provides, in some embodiments, recombinant oncolyticviruses and methods of using said oncolytic viruses for the treatment ofcancer. In some embodiments, the oncolytic viruses of this disclosurecomprise modification in the viral genome encoding exogenous nucleicacids to enhance the oncolytic immunotherapy by remodeling the tumormicroenvironment and with enhanced systemic delivery. The presentdisclosure further relates to the composition of matter comprising suchoncolytic viruses and the method of use and kits for cancer treatments.

Certain Definitions

As used herein, the singular forms “a”, “an” and “the,” may refer toboth the singular as well as plural, unless the context clearlyindicates otherwise. As used herein, the term “comprises” can mean“includes.” Thus, “comprising one or more modifications in the viralgenome” may mean “including at least one of the modifications in theviral” without excluding other elements. In case of conflict, thepresent specification, including explanations of terms, will control. Inaddition, the materials, methods, and examples are illustrative only andnot intended to be limiting. The term “about” or “approximately” canmean within an acceptable error range for the particular value asdetermined by one of ordinary skill in the art, which will depend inpart on how the value is measured or determined, e.g., the limitationsof the measurement system. For example, “about” can mean within 1 ormore than 1 standard deviation, per the practice in the given value.Where particular values are described in the application and claims,unless otherwise stated the term “about” should be assumed to mean anacceptable error range for the particular value, such as ±10% of thevalue modified by the term “about”.

The term “recombinant oncolytic virus” as defined herein include anoncolytic virus strain engineered to delete or functionally delete oneor more endogenous nucleic acid sequences and/or insert or partiallyinsert one or more exogeneous nucleic acid sequences. The term alsoincludes the substitution of the one or more endogenous nucleic acidsequences in a viral genome with the one or more exogeneous nucleic acidat the same or different loci.

The term “effective amount” as used herein, can refer to an amount of anagent (such as a recombinant oncolytic virus disclosed herein, as wellas other anti-cancer agents) that is sufficient to effect beneficial ordesired results. An effective amount (also referred to as atherapeutically effective amount) may vary depending upon one or moreof: the subject and disease condition being treated, the weight and ageof the subject, the severity of the disease condition, the manner ofadministration and the like, which can readily be determined by one ofordinary skill in the art. The beneficial therapeutic effects caninclude, but are not limited to, enablement of diagnosticdeterminations; amelioration of a disease, symptom, disorder, orpathological condition; reducing or preventing the onset of a disease,symptom, disorder or condition; and generally counteracting a disease,symptom, disorder or pathological condition.

Overview

Provided herein are compositions and methods relating to inhibitingmajor histocompatibility complex (MHC) Class I presentation withinvirally infected cells as a means to (i) reduce the immune responsetargeting the virus and virus infected cells while increasing the immuneresponse targeting the surrounding tumor. Further provided herein arecompositions and methods for recombinant oncolytic viruses engineered toactivate major histocompatibility complex (MHC) Class II presentationthroughout the tumor microenvironment, while also helping to overcomeimmune resistance to immune oncology therapies (e.g., immune check pointinhibitor therapies) mediated by tumor-mediated downregulation of MHC IIpresentation.

In some embodiments, the recombinant oncolytic virus is a vacciniavirus, wherein the vaccinia virus can be modified such that the virus(i) is deleted for vaccinia’s natural MHC II inhibitor; and (ii) hasbeen engineered to express an MHC I inhibitor from cowpox virus. It isshown herein, in some aspects, that substitution of vaccinia virus geneWR158 encoding protein A35 (NCBI Accession No. YP_233040) with a DNAsequence encoding viral promoter P7.5 (SEQ ID NO: 1) driving expressionof cowpox protein CPXV012 (NCBI accession No. NP_619801) (SEQ ID NO: 2)or with a DNA sequence encoding cowpox protein CPXV203 can result in agreater therapeutic activity than the same virus without thissubstitution.

In some embodiments, the MHC I inhibitor can be selected from one ormore of TAP inhibitors, such as UL49.5; ICP47; US6, BNLF2a.

In some embodiments, better activation of MHC II presentation can beachieved by other methods including or excluding the deletion ofvaccinia’s natural MHC II inhibitor. These other methods include but arenot limited to modification in the recombinant vaccinia virus such thatthe viral genome is modified by insertion of the gene encoding at leastone of an apoptosis inhibitor protein or a necrotic cell death activatorprotein; an autophagy enhancer protein (e.g., HMGB1); an asparaginylendopeptidase; a class II transactivator (CIITA); an interferon-gamma; aToll-like receptors (TLR) activator; a dendritic cell (DC) maturationactivator (e.g., osteopontin or TNF-alpha) or Fas ligand.

In some embodiments, the inhibition of major histocompatibility complex(MHC) Class I presentation can be achieved by other methods including orexcluding the insertion of a gene from cowpox virus expressing an MHC Iinhibitor. These other methods include but are not limited to insertionof an exogenous gene in the viral genome from one or more of a MHC Iinhibitor derived from a herpesvirus such as Epstein-Barr virus encodednuclear antigen 1 (EBNA1) or BNLF2a proteins, Herpes simplex virusencoded ICP47 or UL49.5 proteins, Herpes simplex virus encoded protein,Human cytomegalovirus (HCMV) encoded US6, US2, US3 US11 or gp48proteins, Epstein-Barr Virus encoded BNLF2a protein, Kaposi’ssarcoma-associated herpesvirus (KSHV) encoded kK3, vIRF3 or kK5 protein,or dominant negative form of IRF7.

Other viral proteins that down regulate MHC I include for exampleAdenovirus encoded E3-19K protein, Human Immunodeficiency Virus 1encoded Nef protein, Human Immunodeficiency Virus 2 encoded Nef protein,and Simian Immunodeficiency Virus 1 encoded Nef protein.

Oncolytic Viruses

Provided herein are compositions comprising an oncolytic virus which ismodified. Modifications include the addition of an exogenous nucleicacid described herein. Further modifications include the addition of agenomic modification as described herein. Exemplary oncolytic virusesfor inclusion in composition described herein include, withoutlimitation, a poxvirus, an adeno associated virus, an adenovirus,Newcastle disease virus (NDV), Reovirus (RV), mengovirus, Myxoma virus(MYXV), Measles virus (MV), Herpes Simplex virus (HSV), Vaccinia virus(VV), Vesicular Stomatitis virus (VSV), and Polio virus (PV). Theseoncolytic viruses have a proclivity to specifically target cancer cells,and upon virus replication cause significant cell death and tumorregression. In some embodiments, oncolytic viruses as described herein,kill cancer or tumor cells through mechanisms such as the direct lysisof said cells, by stimulating immune response towards said cells,apoptosis, expression of toxic proteins, autophagy and shut-down ofprotein synthesis, induction of anti-tumoral immunity, or anycombinations thereof. In some embodiments, the poxvirus comprises abetaentomopoxvirus, a yatapoxvirus, a cervidpoxvirus, agammaentomopoxvirus, a leporipoxvirus, a suipoxvirus, amolluscipoxvirus, a crocodylidpoxvirus, an alphaentomopoxvirus, acapripoxvirus, an avipoxvirus, or a parapoxvirus. In some embodiments,the pox virus comprises a vaccinia virus. In some embodiments, the poxvirus is a vaccinia virus.

Based on these approaches, there is also provided compositions andmethods for tumor therapy such that immune response targeting infectedcells in the tumor is reduced and instead uninfected tumor cells arebetter targeted (e.g., this approach can reduce anti-viral immunity infavor of anti-tumor immune response).

Provided herein are recombinant viruses incorporating genomemodification, including insertions, mutations or deletions, as well asinsertion of exogenous genes described herein. In some embodiments, suchmodifications are generated by spontaneous recombination with a transfervector. For example, the vector, which can be a circular plasmid orlinear DNA fragment, can comprise a desired DNA sequence to be added tothe viral genome followed by a gene encoding a floxxed fluorescentreporter protein under a strong viral promoter. Such components can beflanked by 200 to 1000 bases in length of DNA sequence homologous toviral genomic DNA immediately preceding, and immediately following thedesired integration site, which direct site-specific integration of thevector payload plus reporter. Purified vector DNA is transfected into avirus-susceptible adherent cell line, for example: 143B seeded atapproximately one million cells in a single well of a 6-well cellculture plate. Transfected cells are then infected with a virus intowhich the vector DNA is intended to integrate. Recombination between thevector and viral genome occurs spontaneously during viral replication.One to three days post-infection, recombinant virus (alongside parentalvirus) is harvested from the transfected cells by removing medium andlysing the cell monolayer. Recombinant virus is purified from parentalvirus by plaque selection. Multi-well plates (e.g., 96-well, treated foradherent cell culture) are seeded with between 1.2 × 10⁴ - 3.0 × 10⁴cells per well on the day of plaque selection. Lysate comprising amixture of recombinant and parental virus is sonicated, then diluted incell culture medium and distributed between wells in the top row of aseeded 96-well plate. Medium from the infected row is mixed andtransferred into the next adjacent row of cells in the plate. Theprocess of serial dilution is performed for all rows in the selectionplate. Infected plates are stored in a cell culture incubator for two tothree days to allow plaques to develop. Plaques formed by recombinantvirus are fluorescent due to reporter gene expression and are identifiedusing a fluorescence microscope. Recombinant plaques are picked manuallyusing a single-channel micropipette - typically 0.5 to 3.0 microlitersof material are picked from each plaque. Preferred plaques are round,uniform in reporter intensity, and alone within their well. Pickedplaques are frozen, thawed, then diluted and used to infect additional96-well selection plates. A pure population (wholly GFP-positive) ofrecombinant plaques is achieved after several rounds of selection. Thereporter gene is then deleted from the viral genome by transfectingcells with a vector that encodes cre recombinase under a viral promoter.Transfected cells are infected with reporter-positive virus, allowingexpressed cre to remove the floxxed reporter. Reporter-free virus ispurified by plaque selection in the same manner as previous described,targeting GFP-lacking plaques that are alone in their wells.

Recombinant Vaccinia Viruses

In some embodiments, the oncolytic virus is a vaccinia virus. As usedinterchangeably herein, the term “recombinant vaccinia virus” or a“recombinant vaccinia virus,” can relate to a vaccinia virus that hasbeen modified. Example modifications include, without limitation,introducing viral backbone mutations, to express genes/peptides of avaccinia virus, or deleting genes, where the modification facilitatesamong other things, an increased immune response. In some embodiments,introducing a viral backbone mutation comprises a complete deletion or apartial deletion of one or more virulence genes, or substitutions withone or more viral virulence genes (non-limiting examples include genesthat are known to inhibit cytokines involved in the Th1 immune response,or in innate immune signaling, or inhibitors of other components of theimmune response, or with vaccinia virulence genes exchanged with more orless potent genes of equivalent function from other poxviruses).

Modifications in the genome of the virus can be at one or more locationswithin the genome. In some embodiments, modifications in the genome ofthe virus are located contiguously in the genome. In some embodiments,modifications in the genome of the virus are distributed throughout thegenome.

Exemplary vaccinia viruses include, without limitation, the followingstrains for modification by inclusion of a fusion construct describedherein: Western Reserve Vaccinia virus (ATCC VR-1354), Vaccinia virusAnkara (ATCC VR-1508), Vaccinia virus Ankara (ATCC VR-1566), Vacciniavirus strain Wyeth (ATCC VR-1536), or Vaccinia virus Wyeth (ATCCVR-325). Furthermore, in some embodiments the recombinant vacciniaviruses are modified versions of a wild type or attenuated vacciniavirus strain. Nonlimiting examples of vaccinia virus strains includeWestern Reserve strain of vaccinia virus, Copenhagen strain, Wyeth(NYCBOH) strain, Tian Tan strain, Lister, USSR, Ankara, NYVAC strain,and recombinant vaccinia virus Ankara (MVA). Additional exemplarystrains for inclusion in compositions described herein are, withoutlimitation, Western Reserve strain Vaccinia virus, a Copenhagen strain,an IHD strain, a Wyeth strain, a NYCBOH strain, a Tian Tan strain, aLister strain, an Ankara strain, a USSR strain, or an ACAM2000 strain.The base vaccinia virus strain modified as set forth herein may itselfcomprise one or more mutation relative to its parent strain, forexample, but not limited to, one or more of the following: deletion inTK (also referred to herein as “TK-”); deletion in A52 (also referred toherein as “A52-). An exemplary vaccinia virus is Western Reservevaccinia viruses. Any known vaccinia virus, or modifications thereofthat correspond to those provided herein or known to those of skill inthe art are also covered in the scope of this application.

Modification That Inhibits MHC I Presentation

Presentation of peptides on Major Histocompatibility Complex I, or MHCI, is a pathway in which peptides are presented on cells to alert theimmune system to virally infected cells. For example, an infected cellmay present a viral peptide on MHC I, thereby alerting cytotoxic Tlymphocytes to destroy these cells. Upon infection of a host with arecombinant oncolytic virus, presentation of peptides on MHC I can beinhibited.

Provided herein, in some embodiments of this disclosure, aremodifications of the recombinant oncolytic virus that provide inhibitionor partial inhibition of MHC I presentation. The modification cancomprise an insertion or partial insertion of an exogenous MHC Iinhibitor. The insertion of the MHC I inhibitor can be provided by anexogenous nucleic acid that encodes said MHC I inhibitor. The exogenousnucleic acid encoding said MHC I inhibitor can be inserted into anucleic acid sequence of an oncolytic viral genome such as the cowpoxvirus. In certain instances, the MHC I inhibitor is inserted into anon-coding region. In other instances, the inhibitor is inserted into anucleic acid sequence encoding a viral protein of the oncolytic virus.In certain instances, the MHC I inhibitor is inserted into a region ofthe oncolytic viral genome that allows the virus to replicate in tumorcells. In certain instances, concerning the cowpox virus, the MHC Iinhibitor can be inserted into at least 1, at least 2, at least 3, atleast 4, at least 5, at least 6, at least 7, at least 8, at least 9, orat least 10 genes. The gene encoding the cowpox virus protein can beCPXV012, CPXV203, or any combination thereof. In some embodiments, thecowpox virus protein, including any combinations of substitution,insertion, and deletion, can result in a sequence with less than 100%,99%, 98%, 97%, 96%, 95%, 94%, 93%, 92%, 91%, 90% or less sequencehomology to the wild-type sequence of the viral gene or a viral proteincoded by the gene. MHC I presentation can been decreased by at least 1%,at least 2%, at least 5%, at least 10%, at least 15%, at least 20%, atleast 25%, at least 30%, at least 35%, at least 40%, at least 45%, atleast 50%, at least 55%, at least 65%, at least 70%, at least 75%, atleast 80%, at least 85%, at least 95%, or at least 100%.

The exogenous nucleic acid, in some embodiments, can encode at least oneTAP inhibitor. The exogenous nucleic acid, in some embodiments, canencode at least one gene selected from the group consisting of:Epstein-Barr virus encoded nuclear antigen 1 (EBNA1) protein, Herpessimplex virus encoded ICP47 protein, Herpes simplex virus encoded UL49.5protein, Human cytomegalovirus (HCMV) encoded US6, US2, US3 or US11protein, Epstein-Barr Virus encoded BNLF2a protein, Adenovirus encodedE3-19K protein, Cytomegalovirus encoded gp48 protein, HumanImmunodeficiency Virus encoded Nef protein, Kaposi’s sarcoma-associatedherpesvirus (KSHV) encoded kK3, vIRF3 or kK5 protein or a dominantnegative form of IRF7.

Modification That Activates MHC Class II Presentation

Provided herein, in some embodiments of this disclosure, aremodifications of the recombinant oncolytic virus resulting in activationof MHC II presentation, wherein the modification can comprise at leastone of: i) a deletion or partial deletion of one or more MHC IIinhibitors (e.g., natural MHC II inhibitors); ii) insertion of anapoptosis inhibitor proteins or necrotic cell death activator proteins;or any combination thereof. The modification can be a deletion of anoncolytic virus gene. The modification can be a deletion (a complete ora partial deletion) of A35 encoding gene. The modification of thedeletion of the A35 encoding can be a deletion or functional deletion ofviral gene WR158. In some embodiments, the MHC II inhibitor, includingany combinations of substitution, insertion, and deletion, can result ina sequence with less than 100%, 99%, 98%, 97%, 96%, 95%, 94%, 93%, 92%,91%, 90% or less sequence homology to the wild-type sequence of theviral gene or a viral protein coded by the gene, that is the natural MHCII inhibitor of the virus. MHC II presentation can be activated orenhanced by at least 1%, at least 2%, at least 5%, at least 10%, atleast 15%, at least 20%, at least 25%, at least 30%, at least 35%, atleast 40%, at least 45%, at least 50%, at least 55%, at least 65%, atleast 70%, at least 75%, at least 80%, at least 85%, at least 95%, or atleast 100%, compared to a virus which does not comprise the modificationthat activates or enhances MHC II presentation, but is otherwiseidentical.

The modification causing activation or enhancement of MHC IIpresentation can include insertion of one or more genes selected fromthe group consisting of: an apoptosis inhibitor protein or a necroticcell death activator protein; an autophagy enhancer protein; anasparaginyl endopeptidase; a class II transactivator (CIITA); aninterferon-gamma; a Toll-like receptors (TLR) activator; a dendriticcell (DC) maturation activator (e.g., osteopontin or TNF-alpha). Incertain instances, the MHC II enhancer may be modified to includesecretory sequences and cell permeability domains to provide animmunological bystander effect. In some cases, the autophagy enhancerprotein comprises HMGB1, PIAS3, LIGHT, ITAC, a fractalkine, a functionaldomain or fragment or variant thereof, or any combinations thereof. Insome cases, the autophagy enhancer protein comprises HMGB1. In somecases, the HMGB1 comprises a nucleic acid sequence as set forth in SEQID NO: 4 or an amino acid sequence set forth in SEQ ID NO: 5. In somecases, the secretory sequence comprises an IgE-derived signal sequence.In some cases, the IgE-derived signal sequence comprises a nucleic acidsequence as set forth in SEQ ID NO: 6 or an amino acid sequence setforth in SEQ ID NO: 7. In some cases, the HMGB1 is modified with anIgE-derived signal sequence, wherein the modified HMGB1 comprises anucleic acid sequence as set forth in SEQ ID NO: 8 or an amino acidsequence as set forth in SEQ ID NO: 9.

Concurrent MHC II upregulation (which ideally occurs in non-infectedcells, but that is not a requirement) leads to more efficient targetingof tumor antigens (MHC II downregulation is one of the common tumorresistance mechanisms to anti-PD1/PDL1 antibodies for example).

Provided herein are modifications of the recombinant oncolytic virusthat provide for inhibition or partial inhibition of MHC I presentationas described herein, and further provide for activation of MHC IIpresentation as described herein. In some instances, modifications arein separate locations in the genome. In some instances, modificationsare in the same location in the genome. In some instances, modificationsare in adjacent locations in the genome.

Other Multiple Modifications

Provided herein in some embodiments are vaccines comprising recombinantoncolytic viruses with insertions, mutations or deletions in the viralgenome (also referred to herein as the viral backbone). In the case ofoncolytic vaccinia viruses, they are preferably recombinant or selectedto have low toxicity and to accumulate in the target tissue. In someembodiments, the modifications in the viral backbone/viral genome aremodifications that render the vaccinia virus non-replicating or comprisea poor replicative capacity. Non-limiting examples of such modificationscan include mutations in the following viral genes: TK, A1, A2, VH1,A33, I7, F13L, A36R, A34R, A46R, A49R, B8R, B14R, B15R, B18R, C12L, C4,C16, SPI-1, SPI-2, B15R, VGF, E3L, K1L, K3L, K7R, A41L, M2L, N1L, A52R,a functional domain or fragment or a variant thereof, or anycombinations thereof.

In some embodiments, concerning the vaccinia virus, the viral backbonemutation is selected from the group consisting of: a complete or partialdeletion of the A52R gene; a complete or partial deletion of the TKgene; a complete or partial deletion of the F13L gene; a complete orpartial deletion of the A36R gene; a complete or partial deletion of theA34R gene; a complete or partial deletion of the B8R gene; gene; acomplete or partial deletion of the B18R gene; a complete or partialdeletion of the C12L gene; a complete or partial deletion of the C4gene; a complete or partial deletion of the C16 gene; a complete orpartial deletion of the SPI-1 gene; a complete or partial deletion ofthe SPI-2 gene; a complete or partial deletion of the VGF gene; acomplete or partial deletion of the E3L gene; a complete or partialdeletion of the K3L gene; a complete or partial deletion of the A41Lgene; gene; a complete or partial deletion of the a complete or partialdeletion of the A52R gene; a complete or partial deletion of the B15Rgene; a complete or partial deletion of the K7R gene; a complete orpartial deletion of the B14R gene; a complete or partial deletion of theN1L gene; a complete or partial deletion of the K1L gene; a complete orpartial deletion of the M2L gene; a complete or partial deletion of theA49R gene; a complete or partial deletion of the VH1 gene; a complete orpartial deletion of A33 gene; a complete or partial deletion of A1; acomplete or partial deletion of A2 gene; a complete or partial deletionof I7 gene, and a complete or partial deletion of the A46R gene. As usedherein, the reference to a viral gene can be made by reference to theprotein encoded by the gene (e.g., A33 gene can mean a gene that codesfor the A33 protein).

In some embodiments, the viral backbone mutation of the oncolytic virus,including any combinations of substitution, insertion, and deletion, canresult in a sequence with less than 100%, 99%, 98%, 97%, 96%, 95%, 94%,93%, 92%, 91%, 90% or less sequence homology to the wild-type sequenceof the viral gene or a viral protein coded by the gene. The viral geneand protein coded by the same, in some embodiments, is selected from thegroup consisting of: TK, A1, A2, VH1, A33, I7, F13L, A36R, A34R, A46R,A49R, B8R, B14R, B15R, B18R, C12L, C4, C16, SPI-1, SPI-2, B15R, VGF,E3L, K1L, K3L, K7R, A41L, M2L, N1L, and A52R.

In some embodiments, the viral backbone can comprise 1, 2, 3, 4, 5, ormore mutations in the amino acid sequence of the viral protein (e.g., aviral antigen). The viral antigen is in some examples selected from thegroup consisting of: TK, A1, A2, VH1, A33, I7, F13L, A36R, A34R, A46R,A49R, B8R, B14R, B15R, B18R, C12L, C4, C16, SPI-1, SPI-2, B15R, VGF,E3L, K1L, K3L, K7R, A41L, M2L, N1L, and A52R.

The disclosure provides in some embodiments, recombinant oncolyticviruses comprising one more mutation in the genome of the virus (virusback bone) such that the mutation increases the T-cell arm of the immuneresponse. A mutation may be addition, deletion or substitution of one ormore nucleic acid in the viral genome (wild type or attenuated nativestrains of oncolytic virus).

In non-limiting examples, the mutation can be complete or partialdeletion of genes that are known to inhibit cytokines involved in theTh1 immune response. As non-limiting examples the mutation may bedeletion of nucleic acid encoding B8R (interferon gamma (IFN-g) bindingproteins); C12L (interleukin-18 (IL-18) binding proteins).

In further non-limiting example, the mutation can be complete or partialdeletion of genes in innate immune signaling. As non-limiting examplesthe mutation may be deletion of nucleic acid encoding B18R (type Iinterferon (IFN)-binding proteins); A52R (nuclear factor κB (NF- κB)inhibitor proteins); E3L (protein kinase (PKR) inhibitors); C4, C16(STING pathway inhibitors).

In further non-limiting example, the mutation can be complete or partialdeletion of genes encoding proteins for inhibition of other componentsof the immune response. As non-limiting examples the mutation may be acomplete or partial deletion of nucleic acid encoding B15, K7, B14, N1,K1, M2, A49, VH1, A46 or combination thereof. The viral backbonemutation may also include substituting the oncolytic virulence geneswith mostly potent genes of equivalent function from other poxviruses.

Amino acid sequence variants of the polypeptides of the presentdisclosure can be substitutional, insertional or deletion variants. Amutation in a gene encoding a viral polypeptide may affect 1, 2, 3, 4,5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23,24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41,42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59,60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77,78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95,96, 97, 98, 99, 100, 110, 120, 130, 140, 150, 160, 170, 180, 190, 200,210, 220, 230, 240, 250, 275, 300, 325, 350, 375, 400, 425, 450, 475,500 or more non-contiguous or contiguous amino acids of the polypeptide,as compared to wild-type.

Deletion variants may lack one or more residues of the native orwild-type protein. Individual residues can be deleted or all or part ofa domain (such as a catalytic or binding domain) can be deleted. A stopcodon may be introduced (by substitution or insertion) into an encodingnucleic acid sequence to generate a truncated protein. Insertionalmutants typically involve the addition of material at a non-terminalpoint in the polypeptide. This may include the insertion of animmunoreactive epitope or simply one or more residues. Terminaladditions, called fusion proteins, may also be generated.

Substitutional variants typically comprise the exchange of one aminoacid for another at one or more sites within the protein and may bedesigned to modulate one or more properties of the polypeptide, with orwithout the loss of other functions or properties. Substitutions may beconservative, that is, one amino acid is replaced with one of similarshape and charge. Conservative substitutions can include, for example,the changes of: alanine to serine; arginine to lysine; asparagine toglutamine or histidine; aspartate to glutamate; cysteine to serine;glutamine to asparagine; glutamate to aspartate; glycine to proline;histidine to asparagine or glutamine; isoleucine to leucine or valine;leucine to valine or isoleucine; lysine to arginine; methionine toleucine or isoleucine; phenylalanine to tyrosine, leucine or methionine;serine to threonine; threonine to serine; tryptophan to tyrosine;tyrosine to tryptophan or phenylalanine; and valine to isoleucine orleucine. Alternatively, substitutions may be non-conservative such thata function or activity of the polypeptide is affected. Non-conservativechanges typically involve substituting a residue with one that ischemically dissimilar, such as a polar or charged amino acid for anonpolar or uncharged amino acid, and vice versa.

The oncolytic viruses provided herein comprise additional insertions,mutations, deletions or substitutions in the viral genome. An oncolyticvirus may comprise one or more additional insertions or partialinsertions of exogenous nucleic acids that code for one or more ofchemokine receptor, TRIF protein or a functional domain thereof, or oneor more of leptin, interleukin-2 (IL2), interleukin-15/ interleukin-15Ra(IL15/IL15Ra), interleukin-7 (IL-7), leptin-interleukin fusion protein(e.g. leptin-IL2 fusion protein shown in example 1 as L2). In somecases, the nucleic acid encodes for an IL15 amino acid sequence as setforth in SEQ ID NO: 10. In some cases, the nucleic acid encodes for anIL-7 amino acid sequence as set forth in any of SEQ ID NOs: 13 or 14.Modifications such as insertion of chemokine receptor is insertion ofwild type and/ or mutant type CCL5, CXCR4, CCR2, CCL2. In some cases,the nucleic acid encodes for a CXCR4 amino acid sequence as set forth inany one of SEQ ID NOs: 18-20. In some cases, the nucleic acid encodesfor a CXCR4 amino acid sequence as set forth in SEQ ID NO: 18. In somecases, the nucleic acid encodes for a CCR2 amino acid sequence as setforth in any one of SEQ ID NOs: 23-24. An oncolytic virus may furthercomprise one or more additional deletions or partial deletions of one ormore genes from TK, A1, A2, VH1, A33, I7, F13L, A36R, A34R, A46R, A49R,B8R, B14R, B15R, B18R, C12L, C4, C16, SPI-1, SPI-2, B15R, VGF, E3L, K1L,K3L, K7R, A41L, M2L, N1L, A52R a functional domain or fragment orvariant thereof, or any combinations thereof. In some cases, theoncolytic virus provided herein can comprise a complete or partialdeletion of the A52R gene and an insertion of a chemokine receptor, suchas CCR2. In some cases, the oncolytic virus provided herein can comprisea complete or partial deletion of the A52R gene and an insertion of achemokine receptor, such as CCR2. In some cases, the oncolytic virusprovided herein can comprise a complete or partial deletion of at leastone of: A52R or TK viral genes, and insertion of an exogenous nucleicacid encoding a fusion protein (e.g., a metabolic modulator proteinfused to a cytokine, such as Leptin-IL2 fusion protein).

Hyaluronan (HA) is a structural element of ECM and a high molecularweight linear glycosaminoglycan consisting of repeating disaccharideunits It can be distributed widely throughout connective, epithelial,and neural tissues, and its expression level can be significantlyelevated in many types of tumors. Hyaluronidases are a family of enzymesthat catalyze the degradation of HA. There are at least five functionalhyaluronidases identified so far in human: HYAL1, HYAL2, HYAL3, HYAL4and HYAL5 (also known as PH-20 or SPAM1), among which PH-20 is the onlyone known so far to be functional at relatively neutral pH. In somecases of the present disclosure, combining hyaluronidase with othertumor-targeting therapeutic agents (such as transgenes, also referred toherein as exogenous nucleic acid) can promote the therapeutic effect ofthe modified oncolytic virus at least by diminishing the ECM andenhancing the transportation ofthe therapeutic agent inside and betweenthe tumors.

Some embodiments herein disclose a modified oncolytic virus that cancomprise an exogenous nucleic acid coding for a membrane associatedprotein that is capable of degrading hyaluronan, such as ahyaluronidase. It should be noted that the term “hyaluronidase” as usedherein can refer to any enzyme or a fragment thereof that catalyzes thedegradation of HA in a tumor, including, but not limited to, PH-20 andits homologs fromother species, as well as other engineered/designproteins with similar enzymatic function. As used herein, hyaluronidasecan refer to a class of hyaluronan degrading enzymes. In some cases, thePH-20 comprises an amino acid sequence as described by SEQ ID NO: 26. Insome cases the hyaluronidase comprises an amino acid sequence as setforth in SEQ ID NO: 28. In some cases, the hyaluronidase additionallycomprises a secretory sequence. In some cases, the secretory sequencecomprises an IgE-derived signal sequence. In some cases, the IgE-derivedsignal sequence comprises the amino acid sequence as set forth in SEQ IDNO: 7. In some cases, the hyaluronidase with IgE-derived signal sequencecomprises the nucleic acid sequence set forth in SEQ ID NO: 29 or theamino acid sequence as set forth in SEQ ID NO: 30.

Vaccines, Pharmaceutical Compositions, and Delivery of RecombinantVaccinia Viruses

The present disclosure further provides for pharmaceutical or animmunogenic composition for treatment of a cancer. In addition, thepresent disclosure further provides, in some embodiments, pharmaceuticalor an immunogenic composition that can include a vaccine comprising arecombinant vaccinia virus as described above and suitable carriers. Thevaccine can be provided as a kit which include the recombinant vacciniavirus-based vaccine as described above or a pharmaceutical compositionof recombinant vaccinia virus-based vaccine as described above. Thepharmaceutical compositions for vaccine delivery can be for parenteralor oral delivery or nasal delivery. The pharmaceutical compositions canbe administered to a human at least once. The pharmaceuticalcompositions can be administered to the human more than once.

Also provided herein are recombinant vaccinia viruses, compositions,and/or vaccines comprising a recombinant vaccinia virus for use as amedicament or vaccine.

In some embodiments, a pharmaceutical composition comprising a vaccinecomprising a recombinant vaccinia virus as provided herein can beadministered to a subject at a dose of 10⁶ to 10⁹ PFU, at a dose of 10⁶to 5 × 10⁸ PFU, or 10⁷ to 10⁸ PFU. The recombinant vaccinia virusesprovided herein may also be administered to a subject at a dose of 10⁶,10⁷ PFU, 10⁸, or 5 × 10⁸ PFU. The recombinant vaccinia viruses providedherein can be administered to a human subject at a dose of 10⁷ PFU, 10⁸PFU, or 5 × 10⁸ PFU.

A recombinant vaccinia virus, a vaccine composition, or a pharmaceuticalcomposition as described herein can be formulated in a solution in aconcentration range of 10⁴ to 10⁹ PFU/mL, 10⁵ to 5×10⁸ PFU/mL, 10⁶ to10⁸ PFU/mL, or 10⁷ to 10⁸ PFU/mL. In some embodiments, a vaccinationdose for humans can comprise from about 10⁶ to 10⁹ PFU, including a doseof about 10⁶ PFU, about 10⁷ PFU, or about 10⁸ PFU. In some embodiments,the dose for humans can comprise at least about 2 × 10⁷ PFU, at leastabout 3 × 10⁷ PFU, at least about 5 × 10⁷ PFU, at least about 1 × 10⁸PFU, at least about 2 × 10⁸ PFU, in a volume of 0.1 to 0.5 ml.

The pharmaceutical/immunogenic compositions provided herein maygenerally include one or more pharmaceutically acceptable and/orapproved carriers, additives, antibiotics, preservatives, adjuvants,diluents and/or stabilizers. Such auxiliary substances can be water,saline, glycerol, ethanol, wetting or emulsifying agents, pH bufferingsubstances, or the like. Suitable carriers are typically large, slowlymetabolized molecules such as proteins, polysaccharides, polylacticacids, polyglycolic acids, polymeric amino acids, amino acid copolymers,lipid aggregates, or the like.

A homologous prime-boost regimen may be employed wherein a recombinantvaccinia virus as defined herein can be administered in a first dosage.One or more subsequent administrations of a recombinant vaccinia virusas defined herein can be given to boost the immune response provided inthe first administration. In some embodiments, the one or more antigensdelivered by a recombinant vaccinia virus can be the same or similar tothose of the first administration.

A pharmaceutical composition comprising a recombinant vaccinia virus asprovided herein can be administered to the subject in a single dose, orin multiple (such as 2, 3, 4, etc.) doses. The recombinant vacciniavirus can be administered in a first (priming) and second (boosting)administration. The first dose can comprise from about 10⁶ to about 10⁹PFU/mL of a recombinant vaccinia virus and the second dose can comprisefrom about 10⁶ to about 10⁹ PFU/mL of recombinant vaccinia virus. Thefirst and second dose can comprise at least 1000 PFU/mL of the modifiedvaccine virus.

The second dose of the vaccine or the pharmaceutical/immunogeniccomposition can be administered from 24 hours to about 3 months, such asfrom about 7 days to about 2 months, after the administration of thefirst dose. The second dose can be a booster dose.

The recombinant vaccinia virus or a pharmaceutical/immunogeniccomposition comprising a recombinant vaccinia virus can be administeredintraperitoneally systemically, locally, parenterally, subcutaneously,intravenously, intramuscularly, or intranasally. The vaccine can beadministered with an adjuvant, such as an adjuvant as described herein.

Another aspect of this disclosure relates to a method for affecting animmune response in a subject comprising administering to the subject arecombinant vaccinia virus as escribed herein, a vaccine comprising thesame, or a pharmaceutical/immunogenic composition comprising therecombinant vaccinia virus or the vaccine compositions as describedherein.

An immunization protocol may include immunization with more than oneantigen together in a single dose of the vaccine, multiple doses, andmultiple doses with different antigens in each dose. In someembodiments, an immunization protocol may include immunization with anantigen and an adjuvant. Adjuvants, in the present context, can includecytokines and other immunomodulatory molecules such as TLR (toll likereceptor) agonists and their derivatives that stimulate the immuneresponse.

Also provided herein are method of treating a disease, disorder, orcondition by administering a recombinant vaccinia virus as describedherein. In some embodiments, amount of a recombinant vaccinia virus ofthis disclosure administered to a subject can be between about 10³ and10¹² infectious viral particles or plaque forming units (PFU), orbetween about 10⁵ and 10¹⁰ PFU, or between about 10⁵ and 10⁸ PFU, orbetween about 10⁸ and 10¹⁰ PFU. In some embodiments, the amount of arecombinant vaccinia virus of this disclosure administered to a subjectcan be between about 10³ and 10¹² viral particles or plaque formingunits (PFU), or between about 10⁵ and 10¹⁰ PFU, or between about 10⁵ and10⁸ PFU, or between about 10⁸ and 10¹⁰ PFU. In some embodiments, arecombinant vaccinia virus of this disclosure can be administered at adose that can comprise about 10³ PFU/dose to about 10⁴ PFU/dose, about10⁴ PFU/dose to about 10⁵ PFU/dose, about 10⁵ PFU/dose to about 10⁶PFU/dose, about 10⁷ PFU/dose to about 10⁸ PFU/dose, about 10⁹ PFU/doseto about 10¹⁰ PFU/dose, about 10¹⁰ PFU/dose to about 10¹¹ PFU/dose,about 10¹¹ PFU/dose to about 10¹² PFU/dose, about 10¹² PFU/dose to about10¹³ PFU/dose, about 10¹³ PFU/dose to about 10¹⁴ PFU/dose, or about 10¹⁴PFU/dose to about 10¹⁵ PFU/dose. In some embodiments, a recombinantvaccinia virus of this disclosure can be administered at a dose that cancomprise about 2 × 10³ PFU/dose, 3 × 10³ PFU/dose, 4 × 10³ PFU/dose, 5 ×10³ PFU/dose, 6 × 10³ PFU/dose, 7 × 10³ PFU/dose, 8 × 10³ PFU/dose, 9 ×10³ PFU/dose, about 10⁴ PFU/dose, about 2 × 10⁴ PFU/dose, about 3 × 10⁴PFU/dose, about 4 × 10⁴ PFU/dose, about 5 × 10⁴ PFU/dose, about 6 × 10⁴PFU/dose, about 7 × 10⁴ PFU/dose, about 8 × 10⁴ PFU/dose, about 9 × 10⁴PFU/dose, about 10⁵ PFU/dose, 2 × 10⁵ PFU/dose, 3 × 10⁵ PFU/dose, 4 ×10⁵ PFU/dose, 5 × 10⁵ PFU/dose, 6 × 10⁵ PFU/dose, 7 × 10⁵ PFU/dose, 8 ×10⁵ PFU/dose, 9 × 10⁵ PFU/dose, about 10⁶ PFU/dose, about 2 × 10⁶PFU/dose, about 3 × 10⁶ PFU/dose, about 4 × 10⁶ PFU/dose, about 5 × 10⁶PFU/dose, about 6 × 10⁶ PFU/dose, about 7 × 10⁶ PFU/dose, about 8 × 10⁶PFU/dose, about 9 × 10⁶ PFU/dose, about 10⁷ PFU/dose, about 2 × 10⁷PFU/dose, about 3 × 10⁷ PFU/dose, about 4 × 10⁷ PFU/dose, about 5 × 10⁷PFU/dose, about 6 × 10⁷ PFU/dose, about 7 × 10⁷ PFU/dose, about 8 × 10⁷PFU/dose, about 9 × 10⁷ PFU/dose, about 10⁸ PFU/dose, about 2 × 10⁸PFU/dose, about 3 × 10⁸ PFU/dose, about 4 × 10⁸ PFU/dose, about 5 × 10⁸PFU/dose, about 6 × 10⁸ PFU/dose, about 7 × 10⁸ PFU/dose, about 8 × 10⁸PFU/dose, about 9 × 10⁸ PFU/dose, about 10⁹ PFU/dose, about 2 × 10⁹PFU/dose, about 3 × 10⁹ PFU/dose, about 4 × 10⁹ PFU/dose, about 5 × 10⁹PFU/dose, about 6 × 10⁹ PFU/dose, about 7 × 10⁹ PFU/dose, about 8 × 10⁹PFU/dose, about 9 × 10⁹ PFU/dose, about 10¹⁰ PFU/dose, about 2 × 10¹⁰PFU/dose, about 3 × 10¹⁰ PFU/dose, about 4 × 10¹⁰ PFU/dose, about 5 ×10¹⁰ PFU/dose, about 6 × 10¹⁰ PFU/dose, about 7 × 10¹⁰ PFU/dose, about 8× 10¹⁰ PFU/dose, about 9 × 10¹⁰ PFU/dose, about 10¹⁰ PFU/dose, about 2 ×10¹⁰ PFU/dose, about 3 × 10¹⁰ PFU/dose, about 4 × 10¹⁰ PFU/dose, about 5× 10¹⁰ PFU/dose, about 6 × 10¹⁰ PFU/dose, about 7 × 10¹⁰ PFU/dose, about8 × 10¹⁰ PFU/dose, about 9 × 10¹⁰ PFU/dose, about 10¹¹ PFU/dose, about 2× 10¹¹ PFU/dose, about 3 × 10¹¹ PFU/dose, about 4 × 10¹¹ PFU/dose, about5 × 10¹¹ PFU/dose, about 6 × 10¹¹ PFU/dose, about 7 × 10¹¹ PFU/dose,about 8 × 10¹¹ PFU/dose, about 9 × 10¹¹ PFU/dose, or about 10¹²PFU/dose, about 10¹² PFU/dose to about 10¹³ PFU/dose, about 10¹³PFU/dose to about 10¹⁴ PFU/dose, or about 10¹⁴ PFU/dose to about 10¹⁵PFU/dose. In some embodiments, a recombinant vaccinia virus of thisdisclosure can be administered at a dose that can comprise 3 × 10⁹PFU/dose. In some embodiments, a modified oncolytic vaccinia virus ofthis disclosure can be administered at a dose that can comprise up to 5× 10⁹ PFU/dose.

In some embodiments, a recombinant vaccinia virus of this disclosure,can be administered at a dose that can comprise about 10³ viralparticles/dose to about 10⁴ viral particles /dose, about 10⁴ viralparticles /dose to about 10⁵ viral particles /dose, about 10⁵ viralparticles /dose to about 10⁶ viral particles /dose, about 10⁷ viralparticles /dose to about 10⁸ viral particles /dose, about 10⁹ viralparticles /dose to about 10¹⁰ viral particles /dose, about 10¹⁰ viralparticles /dose to about 10¹¹ viral particles /dose, about 10¹¹ viralparticles /dose to about 10¹² viral particles /dose, about 10¹² viralparticles /dose to about 10¹³ viral particles /dose, about 10¹³ viralparticles /dose to about 10¹⁴ viral particles /dose, or about 10¹⁴ viralparticles /dose to about 10¹⁵ viral particles /dose.

In some embodiments, a recombinant vaccinia virus of this disclosure canbe administered at a dose that can comprise about 10³ PFU/kg to about10⁴ PFU/kg, about 10⁴ PFU/kg to about 10⁵ PFU/kg, about 10⁵ PFU/kg toabout 10⁶ PFU/kg, about 10⁷ PFU/kg to about 10⁸ PFU/kg, about 10⁹ PFU/kgto about 10¹⁰ PFU/kg, about 10¹⁰ PFU/kg to about 10¹¹ PFU/kg, about 10¹¹PFU/kg to about 10¹² PFU/kg, about 10¹² PFU/kg to about 10¹³ PFU/kg,about 10¹³ PFU/kg to about 10¹⁴ PFU/kg, or about 10¹⁴ PFU/kg to about10¹⁵ PFU/kg. In some embodiments, a modified oncolytic vaccinia virus ofthis disclosure can be administered at a dose that can comprise about 2× 10³ PFU/kg, 3 × 10³ PFU/kg, 4 × 10³ PFU/kg, 5 × 10³ PFU/kg, 6 × 10³PFU/kg, 7 × 10³ PFU/kg, 8 × 10³ PFU/kg, 9 × 10³ PFU/kg, about 10⁴PFU/kg, about 2 × 10⁴ PFU/kg, about 3 × 10⁴ PFU/kg, about 4 × 10⁴PFU/kg, about 5 × 10⁴ PFU/kg, about 6 × 10⁴ PFU/kg, about 7 × 10⁴PFU/kg, about 8 × 10⁴ PFU/kg, about 9 × 10⁴ PFU/kg, about 10⁵ PFU/kg, 2× 10⁵ PFU/kg, 3 × 10⁵ PFU/kg, 4 × 10⁵ PFU/kg, 5 × 10⁵ PFU/kg, 6 × 10⁵PFU/kg, 7 × 10⁵ PFU/kg, 8 × 10⁵ PFU/kg, 9 × 10⁵ PFU/kg, about 10⁶PFU/kg, about 2 × 10⁶ PFU/kg, about 3 × 10⁶ PFU/kg, about 4 × 10⁶PFU/kg, about 5 × 10⁶ PFU/kg, about 6 × 10⁶ PFU/kg, about 7 × 10⁶PFU/kg, about 8 × 10⁶ PFU/kg, about 9 × 10⁶ PFU/kg, about 10⁷ PFU/kg,about 2 × 10⁷ PFU/kg, about 3 × 10⁷ PFU/kg, about 4 × 10⁷ PFU/kg, about5 × 10⁷ PFU/kg, about 6 × 10⁷ PFU/kg, about 7 × 10⁷ PFU/kg, about 8 ×10⁷ PFU/kg, about 9 × 10⁷ PFU/kg, about 10⁸ PFU/kg, about 2 × 10⁸PFU/kg, about 3 × 10⁸ PFU/kg, about 4 × 10⁸ PFU/kg, about 5 × 10⁸PFU/kg, about 6 × 10⁸ PFU/kg, about 7 × 10⁸ PFU/kg, about 8 × 10⁸PFU/kg, about 9 × 10⁸ PFU/kg, about 10⁹ PFU/kg, about 2 × 10⁹ PFU/kg,about 3 × 10⁹ PFU/kg, about 4 × 10⁹ PFU/kg, about 5 × 10⁹ PFU/kg, about6 × 10⁹ PFU/kg, about 7 × 10⁹ PFU/kg, about 8 × 10⁹ PFU/kg, about 9 ×10⁹ PFU/kg, about 10¹⁰ PFU/kg, about 2 × 10¹⁰ PFU/kg, about 3 × 10¹⁰PFU/kg, about 4 × 10¹⁰ PFU/kg, about 5 × 10¹⁰ PFU/kg, about 6 × 10¹⁰PFU/kg, about 7 × 10¹⁰ PFU/kg, about 8 × 10¹⁰ PFU/kg, about 9 × 10¹⁰PFU/kg, about 10¹⁰ PFU/kg, about 2 × 10¹⁰ PFU/kg, about 3 × 10¹⁰ PFU/kg,about 4 × 10¹⁰ PFU/kg, about 5 × 10¹⁰ PFU/kg, about 6 × 10¹⁰ PFU/kg,about 7 × 10¹⁰ PFU/kg, about 8 × 10¹⁰ PFU/kg, about 9 × 10¹⁰ PFU/kg,about 10¹¹ PFU/kg, about 2 × 10¹¹ PFU/kg, about 3 × 10¹¹ PFU/kg, about 4× 10¹¹ PFU/kg, about 5 × 10¹¹ PFU/kg, about 6 × 10¹¹ PFU/kg, about 7 ×10¹¹ PFU/kg, about 8 × 10¹¹ PFU/kg, about 9 × 10¹¹ PFU/kg, or about 10¹²PFU/kg, about 10¹² PFU/kg to about 10¹³ PFU/kg, about 10¹³ PFU/kg toabout 10¹⁴ PFU/kg, or about 10¹⁴ PFU/kg to about 10¹⁵ PFU/kg. In someembodiments, a recombinant vaccinia virus of this disclosure can beadministered at a dose that can comprise 3 × 10⁹ PFU/kg. In someembodiments, a recombinant vaccinia virus of this disclosure can beadministered at a dose that can comprise up to 5 × 10⁹ PFU/kg.

In some embodiments, a recombinant vaccinia virus of this disclosure canbe administered at a dose that can comprise about 10³ viral particles/kgto about 10⁴ viral particles/kg, about 10⁴ viral particles/kg to about10⁵ viral particles/kg, about 10⁵ viral particles/kg to about 10⁶ viralparticles/kg, about 10⁷ viral particles/kg to about 10⁸ viralparticles/kg, about 10⁹ viral particles/kg to about 10¹⁰ viralparticles/kg, about 10¹⁰ viral particles/kg to about 10¹¹ viralparticles/kg, about 10¹¹ viral particles/kg to about 10¹² viralparticles/kg, about 10¹² viral particles/kg to about 10¹³ viralparticles/kg, about 10¹³ viral particles/kg to about 10¹⁴ viralparticles/kg, or about 10¹⁴ viral particles/kg to about 10¹⁵ viralparticles/kg.

A liquid dosage form of a recombinant vaccinia virus as described hereincan comprise, in certain embodiments, a viral dose of about 10³ PFU/mLto about 10⁴ PFU/mL, about 10⁴ PFU/mL to about 10⁵ PFU/mL, about 10⁵PFU/mL to about 10⁶ PFU/mL, about 10⁷ PFU/mL to about 10⁸ PFU/mL, about10⁹ PFU/mL to about 10¹⁰ PFU/mL, about 10¹⁰ PFU/mL to about 10¹¹ PFU/mL,about 10¹¹ PFU/mL to about 10¹² PFU/mL, about 10¹² PFU/mL to about 10¹³PFU/mL, about 10¹³ PFU/mL to about 10¹⁴ PFU/mL, or about 10¹⁴ PFU/mL toabout 10¹⁵ PFU/mL. In some embodiments, a recombinant vaccinia virus ofthis disclosure can be administered at a dose that can comprise about 2× 10³ PFU/mL, 3 × 10³ PFU/mL, 4 × 10³ PFU/mL, 5 × 10³ PFU/mL, 6 × 10³PFU/mL, 7 × 10³ PFU/mL, 8 × 10³ PFU/mL, 9 × 10³ PFU/mL, about 10⁴PFU/mL, about 2 × 10⁴ PFU/mL, about 3 ×10⁴ PFU/mL, about 4 × 10⁴ PFU/mL,about 5 × 10⁴ PFU/mL, about 6 × 10⁴ PFU/mL, about 7 × 10⁴ PFU/mL, about8 × 10⁴ PFU/mL, about 9 × 10⁴ PFU/mL, about 10⁵ PFU/mL, 2 × 10⁵ PFU/mL,3 × 10⁵ PFU/mL, 4 × 10⁵ PFU/mL, 5 × 10⁵ PFU/mL, 6 × 10⁵ PFU/mL, 7 × 10⁵PFU/mL, 8 × 10⁵ PFU/mL, 9 × 10⁵ PFU/mL, about 10⁶ PFU/mL, about 2 × 10⁶PFU/mL, about 3 × 10⁶ PFU/mL, about 4 × 10⁶ PFU/mL, about 5 × 10⁶PFU/mL, about 6 × 10⁶ PFU/mL, about 7 × 10⁶ PFU/mL, about 8 × 10⁶PFU/mL, about 9 × 10⁶ PFU/mL, about 10⁷ PFU/mL, about 2 × 10⁷ PFU/mL,about 3 × 10⁷ PFU/mL, about 4 × 10⁷ PFU/mL, about 5 × 10⁷ PFU/mL, about6 × 10⁷ PFU/mL, about 7 × 10⁷ PFU/mL, about 8 × 10⁷ PFU/mL, about 9 ×10⁷ PFU/mL, about 10⁸ PFU/mL, about 2 × 10⁸ PFU/mL, about 3 × 10⁸PFU/mL, about 4 × 10⁸ PFU/mL, about 5 × 10⁸ PFU/mL, about 6 × 10⁸PFU/mL, about 7 × 10⁸ PFU/mL, about 8 × 10⁸ PFU/mL, about 9 × 10⁸PFU/mL, about 10⁹ PFU/mL, about 2 × 10⁹ PFU/mL, about 3 × 10⁹ PFU/mL,about 4 × 10⁹ PFU/mL, about 5 × 10⁹ PFU/mL, about 6 × 10⁹ PFU/mL, about7 × 10⁹ PFU/mL, about 8 × 10⁹ PFU/mL, about 9 × 10⁹ PFU/mL, about 10¹⁰PFU/mL, about 2 × 10¹⁰ PFU/mL, about 3 × 10¹⁰ PFU/mL, about 4 × 10¹⁰PFU/mL, about 5 ×10¹⁰ PFU/mL, about 6 × 10¹⁰ PFU/mL, about 7 × 10¹⁰PFU/mL, about 8 × 10¹⁰ PFU/mL, about 9 × 10¹⁰ PFU/mL, about 10¹⁰ PFU/mL,about 2 × 10¹⁰ PFU/mL, about 3 × 10¹⁰ PFU/mL, about 4 × 10¹⁰ PFU/mL,about 5 × 10¹⁰ PFU/mL, about 6 × 10¹⁰ PFU/mL, about 7 × 10¹⁰ PFU/mL,about 8 × 10¹⁰ PFU/mL, about 9 × 10¹⁰ PFU/mL, about 10¹¹ PFU/mL, about 2× 10¹¹ PFU/mL, about 3 × 10¹¹ PFU/mL, about 4 × 10¹¹ PFU/mL, about 5 ×10¹¹ PFU/mL, about 6 × 10¹¹ PFU/mL, about 7 × 10¹¹ PFU/mL, about 8 ×10¹¹ PFU/mL, about 9 × 10¹¹ PFU/mL, or about 10¹² PFU/mL, about 10¹²PFU/mL to about 10¹³ PFU/mL, about 10¹³ PFU/mL to about 10¹⁴ PFU/mL, orabout 10¹⁴ PFU/mL to about 10¹⁵ PFU/mL. In some embodiments, arecombinant vaccinia virus of this disclosure can be administered at adose that can comprise 5 × 10⁹ PFU/mL. In some embodiments, arecombinant vaccinia virus of this disclosure can be administered at adose that can comprise up to 5 × 10⁹ PFU/mL.

In some instances, where the recombinant vaccinia virus can beadministered by an injection, the dosage can comprise about 10³ viralparticles per injection, 10⁴ viral particles per injection, 10⁵ viralparticles per injection, 10⁶ viral particles per injection, 10⁷ viralparticles per injection, 10⁸ viral particles per injection, 10⁹ viralparticles per injection, 10¹⁰ viral particles per injection, 10¹¹ viralparticles per injection, 10¹² viral particles per injection, 2 × 10¹²viral particles per injection, 10¹³ viral particles per injection, 10¹⁴viral particles per injection, or 10¹⁵ viral particles per injection. Infurther instances, where the recombinant vaccinia virus is administeredby an injection, the dosage can comprise about 10³ infectious viralparticles per injection, 10⁴ infectious viral particles per injection,10⁵ infectious viral particles per injection, 10⁶ infectious viralparticles per injection, 10⁷ infectious viral particles per injection,10⁸ infectious viral particles per injection, 10⁹ infectious viralparticles per injection, 10¹⁰ infectious viral particles per injection,10¹¹ infectious viral particles per injection, 10¹² infectious viralparticles per injection, 2 × 10¹² infectious viral particles perinjection, 10¹³ infectious viral particles per injection, 10¹⁴infectious viral particles per injection, or 10¹⁵ infectious viralparticles per injection. Note that herein 10^(x) is alternativelyexpressed as 1 eX. In certain embodiments, the recombinant vacciniavirus can be administered in one or more doses. In certain embodiments,the virus can be administered in an amount sufficient to induceoncolysis in at least about 20% of cells in a tumor, in at least about30% of cells in a tumor, in at least about 40% of cells in a tumor, inat least about 50% of cells in a tumor, in at least about 60% of cellsin a tumor, in at least about 70% of cells in a tumor, in at least about80% of cells in a tumor, or in at least about 90% of cells in a tumor.

In certain embodiments, a single dose of recombinant virus can refer tothe amount administered to a subject or a tumor over a 1, 2, 5, 10, 15,20, or 24-hour period. In certain embodiments, the dose can be spreadover time or by separate injection. In certain embodiments, multipledoses (e.g., 2, 3, 4, 5, 6 or more doses) of the vaccinia virus can beadministered to the subject, for example, where a second treatment canoccur within 1, 2, 3, 4, 5, 6, 7 days or weeks of a first treatment. Incertain embodiments, multiple doses of the modified oncolytic v can beadministered to the subject over a period of 1, 2, 3, 4, 5, 6, 7 or moredays or weeks. In certain embodiments, the recombinant vaccinia virus orthe pharmaceutical composition as described herein can be administeredover a period of about 1 week to about 2 weeks, about 2 weeks to about 3weeks, about 3 weeks to about 4 weeks, about 4 weeks to about 5 weeks,about 6 weeks to about 7 weeks, about 7 weeks to about 8 weeks, about 8weeks to about 9 weeks, about 9 weeks to about 10 weeks, about 10 weeksto about 11 weeks, about 11 weeks to about 12 weeks, about 12 weeks toabout 24 weeks, about 24 weeks to about 48 weeks, about 48 weeks orabout 52 weeks, or longer. The frequency of administration of therecombinant virus or the pharmaceutical composition as described hereincan be, in certain instances, once daily, twice daily, once every week,once every three weeks, once every four weeks (or once a month), onceevery 8 weeks (or once every 2 months), once every 12 weeks (or onceevery 3 months), or once every 24 weeks (once every 6 months). In someembodiments of the methods disclosed herein, the recombinant vacciniavirus or the pharmaceutical composition can be administered,independently, in an initial dose for a first period of time, anintermediate dose for a second period of time, and a high dose for athird period of time. In some embodiments, the initial dose can be lowerthan the intermediate dose and the intermediate dose can be lower thanthe high dose. In some embodiments of the methods disclosed herein, therecombinant vaccinia virus or the pharmaceutical composition can beadministered, independently, in a high dose for a first period of time,an intermediate dose for a second period of time, and a low dose for athird period of time. In some embodiments, the initial dose can behigher than the intermediate dose and the intermediate dose can behigher than the low dose. In some embodiments, the first, second, andthird periods of time can be, independently, about 1 week to about 2weeks, about 2 weeks to about 3 weeks, about 3 weeks to about 4 weeks,about 4 weeks to about 5 weeks, about 6 weeks to about 7 weeks, about 7weeks to about 8 weeks, about 8 weeks to about 9 weeks, about 9 weeks toabout 10 weeks, about 10 weeks to about 11 weeks, about 11 weeks toabout 12 weeks, about 12 weeks to about 24 weeks, about 24 weeks toabout 48 weeks, about 48 weeks or about 52 weeks, or longer. In someembodiments, a recombinant oncolytic vaccinia virus as described hereincan be administered using a prime-boost regimen.

In some examples, the subject can be put on a reduced carbohydrate diet,e.g., a ketogenic diet prior to, concurrent with, and followingadministration of the modified oncolytic vaccinia virus es or thepharmaceutical composition comprising the same, as described herein,according to any of the methods of treatment described herein. Incertain embodiments, the subject can be put on a diet that can compriseconsuming less than 500 grams of carbohydrates per day, less than 450grams of carbohydrates per day, less than 450 grams of carbohydrates perday, less than 400 grams of carbohydrates per day, less than 350 gramsof carbohydrates per day, less than 300 grams of carbohydrates per day,less than 250 grams of carbohydrates per day, less than 200 grams ofcarbohydrates per day, less than 150 grams of carbohydrates per day,less than 100 grams of carbohydrates per day, less than 90 grams ofcarbohydrates per day, less than 80 grams of carbohydrates per day, lessthan 70 grams of carbohydrates per day, less than 60 grams ofcarbohydrates per day, less than 50 grams of carbohydrates per day, lessthan 40 grams of carbohydrates per day, less than 30 grams ofcarbohydrates per day, less than 20 grams of carbohydrates per day, lessor than 10 grams of carbohydrates per day. An exemplary method for thedelivery of a recombinant vaccinia virus of the present disclosure or apharmaceutical composition comprising the same, to cancer or tumor cellscan be via intratumoral injection. However, alternate methods ofadministration can also be used, e.g., intravenous, via infusion,parenteral, intravenous, intradermal, intramuscular, transdermal,rectal, intraurethral, intravaginal, intranasal, intrathecal, orintraperitoneal. The routes of administration can vary with the locationand nature of the tumor. In certain embodiments, the route ofadministration can be intradental, transdermal, parenteral, intravenous,intramuscular, intranasal, subcutaneous, regional (e.g., in theproximity of a tumor, particularly with the vasculature or adjacentvasculature of a tumor), percutaneous, intrathecal, intratracheal,intraperitoneal, intraarterial, intravesical, intratumoral, inhalation,perfusion, by lavage or orally. An injectable dose of the recombinantvaccinia virus can be administered as a bolus injection or as a slowinfusion. In certain embodiments, the modified oncolytic vaccinia viruscan be administered to the patient from a source implanted in thepatient. In certain embodiments, administration of the modifiedoncolytic vaccinia virus can occur by continuous infusion over aselected period of time. In some instances, a recombinant vaccinia virusas described herein, or a pharmaceutical composition comprising the samecan be administered at a therapeutically effective dose by infusion overa period of about 15 mins, about 30 mins, about 45 mins, about 50 mins,about 55 mins, about 60 minutes, about 75 mins, about 90 mins, about 100mins, or about 120 mins or longer. The recombinant vaccinia virus or thepharmaceutical composition of the present disclosure can be administeredas a liquid dosage, wherein the total volume of administration is about1 mL to about 5 mL, about 5 mL to 10 mL, about 15 mL to about 20 mL,about 25 mL to about 30 mL, about 30 mL to about 50 mL, about 50 mL toabout 100 mL, about 100 mL to 150 mL, about 150 mL to about 200 mL,about 200 mL to about 250 mL, about 250 mL to about 300 mL, about 300 mLto about 350 mL, about 350 mL to about 400 mL, about 400 mL to about 450mL, about 450 mL to 500 mL, about 500 mL to 750 mL, or about 750 mL to1000 mL.

Method of Using Recombinant Oncolytic Virus

The recombinant oncolytic viruses described herein or a pharmaceuticalcomposition or a vaccine comprising the same, as described above, can beused for cancer, in cancer immunotherapy and treatment of tumors. Thetumors can be solid and liquid tumors including but not limited tomelanoma, hepatocellular carcinoma, breast cancer, lung cancer,non-small cell lung cancer, peritoneal cancer, prostate cancer, bladdercancer, ovarian cancer, leukemia, lymphoma, renal cell carcinoma,pancreatic cancer, epithelial carcinoma, gastric/ GE junctionadenocarcinoma, cervical cancer, colon carcinoma, colorectal cancer,duodenal cancer, pancreatic adenocarcinoma, adenoid cystic, sarcoma,mesothelioma, glioblastoma multiforme, astrocytoma, multiple myeloma,prostate carcinoma, hepatocellular carcinoma, cholangiocarcinoma,pancreatic adenocarcinoma, head and neck squamous cell carcinoma,cervical squamous-cell carcinoma, osteosarcoma, epithelial ovariancarcinoma, acute lymphoblastic lymphoma or myeloproliferative neoplasms.As such, some embodiments of this disclosure provide a method oftreatment of a cancer, a tumor, a cancer immunotherapy, by administeringa recombinant oncolytic virus as described herein, or a pharmaceuticalor immunogenic composition comprising the same.

The recombinant vaccinia virus described herein or a pharmaceuticalcomposition or a vaccine comprising the same, as described above, can beused for treating cancer, in cancer immunotherapy and treatment oftumors. The tumors can be solid and liquid tumors including but notlimited to melanoma, hepatocellular carcinoma, breast cancer, lungcancer, non-small cell lung cancer, peritoneal cancer, prostate cancer,bladder cancer, ovarian cancer, leukemia, lymphoma, renal cellcarcinoma, pancreatic cancer, epithelial carcinoma, gastric/ GE junctionadenocarcinoma, cervical cancer, colon carcinoma, colorectal cancer,duodenal cancer, pancreatic adenocarcinoma, adenoid cystic, sarcoma,mesothelioma, glioblastoma multiforme, astrocytoma, multiple myeloma,prostate carcinoma, hepatocellular carcinoma, cholangiocarcinoma,pancreatic adenocarcinoma, head and neck squamous cell carcinoma,cervical squamous-cell carcinoma, osteosarcoma, epithelial ovariancarcinoma, acute lymphoblastic lymphoma or myeloproliferative neoplasms.As such, some embodiments of this disclosure provide a method oftreatment of a cancer, a tumor, a cancer immunotherapy, by administeringa recombinant vaccinia virus as described herein, or a pharmaceutical orimmunogenic composition comprising the same.

Cancer cells that can be treated by the methods of this disclosureinclude cells from the bladder, blood, bone, bone marrow, brain, breast,colon, esophagus, gastrointestine, gum, head, kidney, liver, lung,nasopharynx, neck, ovary, prostate, skin, stomach, testis, tongue, oruterus. In addition, the cancer may specifically be of the followinghistological type, though it is not limited to these: neoplasm,malignant; carcinoma; carcinoma, undifferentiated; giant and spindlecell carcinoma; small cell carcinoma; papillary carcinoma; squamous cellcarcinoma; lymphoepithelial carcinoma; basal cell carcinoma; pilomatrixcarcinoma; transitional cell carcinoma; papillary transitional cellcarcinoma; adenocarcinoma; gastrinoma, malignant; cholangiocarcinoma;hepatocellular carcinoma; combined hepatocellular carcinoma andcholangiocarcinoma; trabecular adenocarcinoma; adenoid cystic carcinoma;adenocarcinoma in adenomatous polyp; adenocarcinoma, familial polyposiscoli; solid carcinoma; carcinoid tumor, malignant; branchiolo-alveolaradenocarcinoma; papillary adenocarcinoma; chromophobe carcinoma;acidophil carcinoma; oxyphilic adenocarcinoma; basophil carcinoma; clearcell adenocarcinoma; granular cell carcinoma; follicular adenocarcinoma;papillary and follicular adenocarcinoma; nonencapsulating sclerosingcarcinoma; adrenal cortical carcinoma; endometroid carcinoma; skinappendage carcinoma; apocrine adenocarcinoma; sebaceous adenocarcinoma;ceruminous adenocarcinoma; mucoepidermoid carcinoma; cystadenocarcinoma;papillary cystadenocarcinoma; papillary serous cystadenocarcinoma;mucinous cystadenocarcinoma; mucinous adenocarcinoma; signet ring cellcarcinoma; infiltrating duct carcinoma; medullary carcinoma; lobularcarcinoma; inflammatory carcinoma; Paget’s disease, mammary; acinar cellcarcinoma; adenosquamous carcinoma; adenocarcinoma w/squamousmetaplasia; thymoma, malignant; ovarian stromal tumor, malignant;thecoma, malignant; granulosa cell tumor, malignant; androblastoma,malignant; sertoli cell carcinoma; leydig cell tumor, malignant; lipidcell tumor, malignant; paraganglioma, malignant; extra-mammaryparaganglioma, malignant; pheochromocytoma; glomangiosarcoma; malignantmelanoma; amelanotic melanoma; superficial spreading melanoma; malignantmelanoma in giant pigmented nevus; epithelioid cell melanoma; bluenevus, malignant; sarcoma; fibrosarcoma; fibrous histiocytoma,malignant; myxosarcoma; liposarcoma; leiomyosarcoma; rhabdomyosarcoma;embryonal rhabdomyosarcoma; alveolar rhabdomyosarcoma; stromal sarcoma;mixed tumor, malignant; mullerian mixed tumor; nephroblastoma;hepatoblastoma; carcinosarcoma; mesenchymoma, malignant; brenner tumor,malignant; phyllodes tumor, malignant; synovial sarcoma; mesothelioma,malignant; dysgerminoma; embryonal carcinoma; teratoma, malignant;struma ovarii, malignant; choriocarcinoma; mesonephroma, malignant;hemangiosarcoma; hemangioendothelioma, malignant; Kaposi’s sarcoma;hemangiopericytoma, malignant; lymphangiosarcoma; osteosarcoma;juxtacortical osteosarcoma; chondrosarcoma; chondroblastoma, malignant;mesenchymal chondrosarcoma; giant cell tumor of bone; Ewing’s sarcoma;odontogenic tumor, malignant; ameloblastic odontosarcoma; ameloblastoma,malignant; ameloblastic fibrosarcoma; pinealoma, malignant; chordoma;glioma, malignant; ependymoma; astrocytoma; protoplasmic astrocytoma;fibrillary astrocytoma; astroblastoma; glioblastoma; oligodendroglioma;oligodendroblastoma; primitive neuroectodermal; cerebellar sarcoma;ganglioneuroblastoma; neuroblastoma; retinoblastoma; olfactoryneurogenic tumor; meningioma, malignant; neurofibrosarcoma;neurilemmoma, malignant; granular cell tumor, malignant; malignantlymphoma; Hodgkin’s disease; Hodgkin’s; paragranuloma; malignantlymphoma, small lymphocytic; malignant lymphoma, large cell, diffuse;malignant lymphoma, follicular; mycosis fungoides; other specifiednon-Hodgkin’s lymphomas; malignant histiocytosis; multiple myeloma; mastcell sarcoma; immunoproliferative small intestinal disease; leukemia;lymphoid leukemia; plasma cell leukemia; erythroleukemia; lymphosarcomacell leukemia; myeloid leukemia; basophilic leukemia; eosinophilicleukemia; monocytic leukemia; mast cell leukemia; megakaryoblasticleukemia; myeloid sarcoma; and hairy cell leukemia. In some cases, solidcancers that are metastatic can be treated using the recombinantoncolytic viruses of this disclosure, such as a recombinant oncolyticvaccinia virus that is advantageous for systemic delivery. In somecases, solid cancers that are inaccessible or difficult to access, suchas for purpose of intratumoral delivery of therapeutic agents, can betreated using the recombinant oncolytic viruses of this disclosure, suchas a recombinant oncolytic virus that is advantageous for systemicdelivery. Cancers that are associated with increased expression of freefatty acids can, in some examples, can be treated using the recombinantoncolytic viruses of this disclosure, such as a recombinant oncolyticvaccinia virus that is advantageous for systemic delivery and formsincreased amounts of EEV.

Combination Therapies

The methods of this disclosure comprise, in some aspects, administeringa recombinant oncolytic virus as disclosed herein or a pharmaceutical oran immunogenic composition comprising the same, followed by, preceded byor in combination with one or more further therapy. Examples of thefurther therapy can include, but are not limited to, chemotherapy,radiation, oncolytic viral therapy with an additional virus, treatmentwith immunomodulatory proteins, an anti-cancer agent, or anycombinations thereof. The further therapy can be administeredconcurrently or sequentially with respect to administration of themodified virus, such as oncolytic vaccinia virus. In certainembodiments, the methods of this disclosure can comprise administering amodified oncolytic virus as disclosed herein, followed by, preceded by,or in combination with one or more anti-cancer agents or cancertherapies. Anti-cancer agents can include, but are not limited to,chemotherapeutic agents, radiotherapeutic agents, cytokines, immunecheckpoint inhibitors, anti-angiogenic agents, apoptosis-inducingagents, anti-cancer antibodies and/or anti-cyclin-dependent kinaseagents. In certain embodiments, the cancer therapies can includechemotherapy, biological therapy, radiotherapy, immunotherapy, hormonetherapy, anti-vascular therapy, cryotherapy, toxin therapy and/orsurgery or combinations thereof. In certain embodiments, the methods ofthis disclosure can include administering a recombinant virus, disclosedherein, followed by, preceded by or in combination with a modifiedoncolytic virus of this disclosure.

In certain embodiments, treatment using a recombinant oncolytic viruscan be used alone or in combination with one or immunomodulatory agents.An immunomodulatory agent can include any compound, molecule orsubstance capable of suppressing antiviral immunity associated with atumor or cancer. In certain embodiments, the immunomodulatory agent canbe capable of suppressing innate immunity or adaptive immunity to themodified virus. Non-limiting examples of immunomodulatory agents includeanti-CD33 antibody or variable region thereof, an anti-CD11b antibody orvariable region thereof, a COX2 inhibitor, e.g., celecoxib, cytokines,such as IL-12, GM-CSF, IL-2 (having an amino acid sequence as set forthin either SEQ ID NO: 33 or 34), IFN3 and IFN-g, and chemokines, such asMIP-1, MCP-1 and IL-8. In certain embodiments, the immunomodulatoryagent can include immune checkpoint modulators such as, but not limitedto, anti-CTLA4, anti-PD-1, and anti-PD-L1 and TLR agonists (e.g., PolyI:C). In some examples, the immunomodulatory agent can include an immunecheckpoint inhibitor, such as an antagonist of PD-1 (e.g., an antagonistantibody that binds to PD-1), an antagonist of PD-L1 (e.g., anantagonist antibody that binds to PD-L1), an antagonist of CTLA-4 (e.g.,an antagonist antibody that binds to CTLA-4), an antagonist of A2AR(e.g., an antagonist antibody that binds to A2AR), an antagonist ofB7-H3 (e.g., an antagonist antibody that binds to B7-H3), an antagonistof B7-H4 (e.g., an antagonist antibody that binds to B7-H4), anantagonist of BTLA (e.g., an antagonist antibody that binds to BTLA), anantagonist of IDO (e.g., an antagonist antibody that binds to IDO), anantagonist of KIR (e.g., an antagonist antibody that binds to KIR), anantagonist of LAG3 (e.g., an antagonist antibody that binds to LAG3), anantagonist of TIM-3 (e.g., an antagonist antibody that binds to TIM3).In some embodiments, the further therapy can comprise administering animmune checkpoint regulator. In one example, the immune checkpointregulator can be TGN1412. In one example, the immune checkpointregulator can be NKTR-214. In one example, the immune checkpointregulator can be MEDI0562. In one example, the immune checkpointregulator can be MEDI6469. In one example, the immune checkpointregulator can be MEDI6383. In one example, the immune checkpointregulator can be JTX-2011. In one example, the immune checkpointregulator can be pembrolizumab. In one example, the immune checkpointregulator can be nivolumab. In one example, the immune checkpointregulator can be ipilimumab. In one example, the immune checkpointregulator can be tremelimumab. In one example, the immune checkpointregulator can be atezolizumab. In one example, the immune checkpointregulator can be MGA271. In one example, the immune checkpoint regulatorcan be indoximod. In one example, the immune checkpoint regulator can beepacadostat. In one example, the immune checkpoint regulator can belirilumab. In one example, the immune checkpoint regulator can beBMS-986016. In one example, the immune checkpoint regulator can beMPDL3280A. In one example, the immune checkpoint regulator can beavelumab. In one example, the immune checkpoint regulator can bedurvalumab. In one example, the immune checkpoint regulator can beMEDI4736. In one example, the immune checkpoint regulator can beMEDI4737. In one example, the immune checkpoint regulator can be TRX518.In one example, the immune checkpoint regulator can be MK-4166. In oneexample, the immune checkpoint regulator can be urelumab (BMS-663513).In one example, the immune checkpoint regulator can be PF-05082566(PF-2566).

In certain examples, where the further therapy is radiation exemplarydoses can be 5,000 Rads (50 Gy) to 100,000 Rads (1000 Gy), or 50,000Rads (500 Gy), or other appropriate doses within the recited ranges.Alternatively, the radiation dose can be about 30 to 60 Gy, about 40 toabout 50 Gy, about 40 to 48 Gy, or about 44 Gy, or other appropriatedoses within the recited ranges, with the dose determined, example, bymeans of a dosimetry study as described above. “Gy” as used herein canrefer to a unit for a specific absorbed dose of radiation equal to 100Rads. Gy is the abbreviation for “Gray.”

In certain examples, where the further therapy is chemotherapy,exemplary chemotherapeutic agents can include without limitationalkylating agents (e.g., nitrogen mustard derivatives, ethylenimines,alkylsulfonates, hydrazines and triazines, nitrosureas, and metalsalts), plant alkaloids (e.g., vinca alkaloids, taxanes,podophyllotoxins, and camptothecan analogs), antitumor antibiotics(e.g., anthracyclines, chromomycins, and the like), antimetabolites(e.g., folic acid antagonists, pyrimidine antagonists, purineantagonists, and adenosine deaminase inhibitors), topoisomerase Iinhibitors, topoisomerase II inhibitors, and miscellaneousantineoplastics (e.g., ribonucleotide reductase inhibitors,adrenocortical steroid inhibitors, enzymes, antimicrotubule agents, andretinoids). Exemplary chemotherapeutic agents can include, withoutlimitation, anastrozole, bicalutamide, bleomycin sulfate, busulfan,busulfan injection, capecitabine,N4-pentoxycarbonyl-5-deoxy-5-fluorocytidine, carboplatin, carmustine,chlorambucil, cisplatin, cladribine, cyclophosphamide, cytarabine,cytosine arabinoside, cytarabine liposome injection, dacarbazine,dactinomycin, daunorubicin hydrochloride, daunorubicin citrate liposomeinjection, dexamethasone, docetaxel, doxorubicin hydrochloride,etoposide, fludarabine phosphate, 5-fluorouracil, flutamide,tezacitibine, gemcitabine (difluorodeoxycitidine), hydroxyurea,Idarubicin, ifosfamide, irinotecan, L-asparaginase, leucovorin calcium,melphalan, 6-mercaptopurine, methotrexate, mitoxantrone, mylotarg,paclitaxel, phoenix, pentostatin, polifeprosan 20 with carmustineimplant, tamoxifen citrate, teniposide, 6-thioguanine, thiotepa,tirapazamine, topotecan hydrochloride for injection, vinblastine,vincristine, and vinorelbine, ibrutinib, idelalisib, and brentuximabvedotin.

Exemplary alkylating agents can include, without limitation, nitrogenmustards, ethylenimine derivatives, alkyl sulfonates, nitrosoureas andtriazenes such as: uracil mustard chlormethine, cyclophosphamide,ifosfamide, melphalan, Chlorambucil, pipobroman, triethylenemelamine,triethylenethiophosphoramine, Temozolomide, thiotepa, busulfan, anddacarbazine. Additional exemplary alkylating agents include, withoutlimitation, oxaliplatin, temozolomide, dactinomycin, L-PAM,L-sarcolysin, hexamethylmelamine, carmustine, bendamustine, busulfan;carboplatin, lomustine, cisplatin, chlorambucil, cyclophosphamide,dacarbazine, altretamine, ifosfamide, prednumustine, procarbazine,mechlorethamine, streptozocin, thiotepa, cyclophosphamide; andbendamustine HCl .

Exemplary anthracyclines can include, without limitation, e.g.,doxorubicin, bleomycin, daunorubicin, daunomycin, rubidomycinhydrochloride, mitoxantrone, epirubicin, idarubicin, mitomycin C,geldanamycin, herbimycin, ravidomycin, and desacetylravidomycin.

Exemplary vinca alkaloids can include, but are not limited to,vinorelbine tartrate, vincristin, vindesine, vinblastine; andvinorelbine.

Exemplary proteasome inhibitors can, but are not limited to, bortezomib; carfilzomib (PX-171-007,(S)-4-Methyl-N-((S)-1-(((S)-4-methyl-1-((R)-2-methyloxiran-2-yl)-1-oxopentan-2-yl)amino)-1-oxo-3-phenylpropan-2-yl)-2-((S)-2-(2-morpholinoac-etamido)-4-phenylbutanamido)-pentanamide),marizomib (NPI-0052), ixazomib citrate, delanzomib, andO-Methyl-N-[(2-methyl-5-thiazolyl)carbonyl]-L-seryl-O-methyl-N-[(1S)-2-[(2R)-2-methyl-2-oxiranyl]-2-oxo-1-(phenylmethyl)ethyl]-L-serinamide.

“In combination with,” as used herein, can mean that the recombinantvirus, such as an oncolytic vaccinia virus as described herein or apharmaceutical composition comprising the same, and the further therapy,such as a further therapy comprising one or more agents are administeredto a subject as part of a treatment regimen or plan. In certainembodiments, being used in combination may not require that therecombinant virus and the one or more agents are physically combinedprior to administration or that they be administered over the same timeframe. For example, and not by way of limitation, the recombinant virusand the one or more agents can be administered concurrently to thesubject being treated or can be administered at the same time orsequentially in any order or at different points in time.

The further therapy can be administered, in various embodiments, in aliquid dosage form, a solid dosage form, a suppository, an inhalabledosage form, an intranasal dosage form, in a liposomal formulation, adosage form comprising nanoparticles, a dosage form comprisingmicroparticles, a polymeric dosage form, or any combinations thereof. Incertain embodiments, the further therapy is administered over a periodof about 1 week to about 2 weeks, about 2 weeks to about 3 weeks, about3 weeks to about 4 weeks, about 4 weeks to about 5 weeks, about 6 weeksto about 7 weeks, about 7 weeks to about 8 weeks, about 8 weeks to about9 weeks, about 9 weeks to about 10 weeks, about 10 weeks to about 11weeks, about 11 weeks to about 12 weeks, about 12 weeks to about 24weeks, about 24 weeks to about 48 weeks, about 48 weeks or about 52weeks, or longer. The frequency of administration of the further therapycan be, in certain instances, once daily, twice daily, once every week,once every three weeks, once every four weeks (or once a month), onceevery 8 weeks (or once every 2 months), once every 12 weeks (or onceevery 3 months), or once every 24 weeks (once every 6 months). Incertain embodiments, a method of treating a subject having a cancer caninclude administering, to the subject, an effective amount of arecombinant virus, e.g., a recombinant vaccinia virus, of thisdisclosure. In certain embodiments, the methods of this disclosure canfurther include administering to the subject an effective amount of oneor more agents. For example, and not by way of limitation, the agent canbe an anti-cancer agent, an immunomodulatory agent, or any combinationsthereof, as described above. An “anti-cancer agent,” as used herein, canbe any molecule, compound, chemical or composition that has ananti-cancer effect. Anti-cancer agents include, but are not limited to,chemotherapeutic agents, radiotherapeutic agents, cytokines, immunecheckpoint inhibitors, anti-angiogenic agents, apoptosis-inducingagents, anti-cancer antibodies and/or anti-cyclin-dependent kinaseagents.

Additional Embodiments

Provided herein are recombinant oncolytic viruses comprising amodification in the viral genome wherein said modification comprises atleast one of: a deletion or functional deletion of an endogenous nucleicacid encoding an MHC class II inhibitor; an insertion of an exogenousnucleic acid that results in activation or enhanced activation of MHCclass II presentation; and an insertion of an exogenous nucleic acidencoding an MHC class I inhibitor that acts wholly or primarily withinthe infected cell. Further provided herein are recombinant oncolyticviruses comprising the deletion or functional deletion of an endogenousnucleic acid encoding the MHC class II inhibitor, wherein the deletionor functional deletion results in an increase of MHC class IIpresentation, and wherein the oncolytic virus is a vaccinia virus.Further provided herein are recombinant oncolytic viruses comprising thedeletion or functional deletion of the endogenous nucleic acid encodingthe MHC class II inhibitor, wherein the deletion or functional deletionof the endogenous nucleic acid encoding the MHC class II inhibitorcomprises a deletion of a gene encoding protein A35 of a vaccinia virus.Further provided herein are recombinant oncolytic viruses wherein thedeletion or functional deletion of the gene encoding a vaccinia virusprotein A35 is a deletion or functional deletion of gene WR158. Furtherprovided herein are recombinant oncolytic viruses wherein themodification comprises the insertion of an exogenous nucleic acid thatresults in activation or enhanced activation of the MHC class IIpresentation, and wherein the exogenous nucleic acid encodes for: anapoptosis inhibitor protein or a necrotic cell death activator protein;an autophagy enhancer protein; an asparaginyl endopeptidase; a class IItransactivator; an interferon-gamma; a Toll-like receptor activator; ora dendritic cell maturation activator. Further provided herein arerecombinant oncolytic viruses comprising the autophagy enhancer protein,wherein the autophagy enhancer protein is HMGB1 or a functional domainor a variant thereof. Further provided herein are recombinant oncolyticviruses comprising the dendritic cell maturation activator, wherein thedendritic cell maturation activator comprises osteopontin, or TNF-alpha,or functional fragments or variants thereof. Further provided herein arerecombinant oncolytic viruses wherein the encoded MHC II upregulatingprotein is fused to a secretion sequence a cell permeabilizing domain ora combination thereof, to achieve MHC II upregulation throughout thetumor. Further provided herein are recombinant oncolytic viruses whereinthe modification comprises the insertion of the exogenous nucleic acidencoding the MHC class I inhibitor, and wherein the insertion results inan inhibition or partial inhibition of MHC class I presentation. Furtherprovided herein are recombinant oncolytic viruses wherein the insertionof the exogenous nucleic acid encoding the MHC class I inhibitorcomprises insertion of a gene encoding one or more cowpox virusproteins. Further provided herein are recombinant oncolytic viruseswherein the insertion of an exogenous nucleic acid encoding the MHCclass I inhibitor comprises insertion of a gene encoding cowpox proteinCPXV012 or a functional fragment or a variant thereof. Further providedherein are recombinant oncolytic viruses wherein the insertion of anexogenous nucleic acid encoding the MHC class I inhibitor comprisesinsertion of a gene encoding cowpox protein CPXV203 or a functionalfragment or a variant thereof. Further provided herein are recombinantoncolytic viruses wherein the insertion of an exogenous nucleic acidencoding the MHC class I inhibitor comprises insertion of a geneencoding at least one of: Epstein-Barr virus encoded nuclear antigen 1protein; Herpes simplex virus encoded ICP47 protein; Herpes simplexvirus encoded UL49.5 protein; Cytomegalovirus encoded US6, US2, US3,US11, or gp48 protein; Epstein-Barr Virus encoded BNLF2a protein;Adenovirus encoded E3-19K protein; Human Immunodeficiency Virus orSimian Immunodeficiency Virus encoded Nef protein; Kaposi’ssarcoma-associated herpesvirus encoded kK3, vIRF3 or kK5 protein; or adominant negative form of IRF7 or IRF3. Further provided herein arerecombinant oncolytic viruses wherein the MHC class I inhibitorcomprises a TAP inhibitor. Further provided herein are recombinantoncolytic viruses wherein the TAP inhibitor acts wholly or primarilywithin infected cells. Further provided herein are recombinant oncolyticviruses wherein the modification in the viral genome reduces an immuneresponse targeting a virus-infected tumor cell and increases an immuneresponse targeting cells surrounding the virus-infected tumor cell.Further provided herein are recombinant oncolytic viruses wherein athymidine kinase gene is deleted from the viral genome. Further providedherein are recombinant oncolytic viruses further comprising an exogenousnucleic acid encoding a hyaluronidase. Further provided herein arerecombinant oncolytic viruses wherein the hyaluronidase is PH-20 orHysA. Further provided herein are recombinant oncolytic viruses whereinthe oncolytic virus is a vaccinia virus, and the vaccinia virus is aWestern Reserve strain Vaccinia virus (ATCC VR-1354), a Copenhagenstrain, an IHD strain, a Wyeth strain (ATCC VR-325), a NYCBOH strain, aTian Tan strain, a Lister strain, an Ankara strain (ATCC VR-1508 or ATTCVR1566), a USSR strain, or an ACAM2000 strain.

Provided herein are recombinant oncolytic viruses comprising amodification in the viral genome wherein the modification comprises adeletion or functional deletion of a vaccinia virus gene encoding A35protein and insertion of an exogenous gene encoding cowpox proteinCPXV012 or cowpox protein CPXV203. Further provided herein arerecombinant oncolytic viruses wherein the modification is such thatinsertion of the exogenous gene encoding cowpox protein CPXV012 is atthe locus of the gene encoding A35 protein of a vaccinia virus. Furtherprovided herein are recombinant oncolytic viruses wherein themodification is such that insertion of the exogenous gene encodingcowpox protein CPXV203 is at the locus of the gene encoding A35 proteinof a vaccinia virus. Further provided herein are recombinant oncolyticviruses further comprising an additional modification in the viralgenome. Further provided herein are recombinant oncolytic viruseswherein the additional modification comprises at least one of: aninsertion of an exogenous nucleic acid that codes for a chemokinereceptor or a functional domain or a variant thereof, or an insertion ofan exogenous nucleic acid that codes for cytokine or a functional domainor a variant thereof. Further provided herein are recombinant oncolyticviruses comprising the exogenous nucleic acid that codes for a cytokineor a functional domain or a variant thereof, wherein the cytokinecomprises at least one of: interleukin-2 (IL-2), interleukin-15/interleukin-15Ra (IL15/IL15Ra), interleukin-7 (IL-7), or a functionaldomain or a variant thereof. Further provided herein are recombinantoncolytic viruses wherein the additional modification comprises aninsertion of an exogenous nucleic acid that codes for a fusion proteincomprising a cytokine and a metabolic modulator protein. Furtherprovided herein are recombinant oncolytic viruses comprising theexogenous nucleic acid that codes for the chemokine receptor or afunctional domain or a variant thereof, wherein the chemokine receptorcomprises at least one of: CXCR4, CCR2, or functional domains orvariants thereof. Further provided herein are recombinant oncolyticviruses wherein the chemokine receptor comprises the CXCR4 or afunctional domain or a variant thereof. Further provided herein arerecombinant oncolytic viruses wherein the chemokine receptor comprisesthe CCR2 or a functional domain or a variant thereof, wherein the CCR2comprises a wild-type CCR2 or a mutated CCR2. Further provided hereinare recombinant oncolytic viruses wherein the exogenous nucleic acidthat codes for the chemokine receptor or a functional domain or avariant thereof comprises a codon optimized sequence. Further providedherein are recombinant oncolytic viruses wherein the exogenous nucleicacid that codes for the chemokine receptor or a functional domain or avariant thereof comprises a non-codon optimized sequence. Furtherprovided herein are recombinant oncolytic viruses wherein the additionalmodification comprises mutation or a complete or a partial deletion of aviral gene comprising at least one of: A52R, B15R, K7R, A46R, N1L, E3L,K1L, M2L, C16, N2R, B8R, B18R, VH1 of a vaccinia virus or a functionaldomain or fragment or variant thereof, or any combinations thereof.Further provided herein are recombinant oncolytic viruses wherein athymidine kinase gene is deleted from the viral genome. Further providedherein are recombinant oncolytic viruses further comprising an exogenousnucleic acid encoding a hyaluronidase. Further provided herein arerecombinant oncolytic viruses wherein the hyaluronidase is PH-20 orHysA. Further provided herein are recombinant oncolytic viruses whereinthe oncolytic virus is a vaccinia virus, and the vaccinia virus is aWestern Reserve strain Vaccinia virus (ATCC VR-1354), a Copenhagenstrain, an IHD strain, a Wyeth strain (ATCC VR-325), a NYCBOH strain, aTian Tan strain, a Lister strain, an Ankara strain (ATCC VR-1508 or ATTCVR1566), a USSR strain, or an ACAM2000 strain.

Provided herein are immunogenic compositions comprising a recombinantoncolytic virus according to any embodiments as described herein.

Provided herein are pharmaceutical compositions comprising a recombinantoncolytic virus or an immunogenic composition according to anyembodiments as described herein and at least one of: a solubilizingagent, an excipient, or a pharmaceutically acceptable carrier. Furtherprovided herein are pharmaceutical compositions, wherein the excipientcomprises one or more of a buffering agent, a stabilizer, anantioxidant, a binder, a diluent, a dispersing agent, a rate controllingagent, a lubricant, a glidant, a disintegrant, a plasticizer, apreservative, or any combinations thereof. Further provided herein arepharmaceutical compositions, wherein the excipient comprises di-sodiumhydrogen phosphate dihydrate, sodium dihydrogen phosphate dihydrate,sodium chloride, myo-inositol, sorbitol, or any combinations thereof.Further provided herein are pharmaceutical compositions, wherein thepharmaceutical composition does not comprise a preservative. Furtherprovided herein are pharmaceutical compositions, further comprising oneor more of a preservative, a diluent, and a carrier. Further providedherein are pharmaceutical compositions, further comprising an additionalactive ingredient or a salt thereof. Further provided herein arepharmaceutical compositions, wherein the solubilizing agent is sterilewater. Further provided herein are pharmaceutical compositions, furthercomprising an additional active ingredient, wherein the additionalactive ingredient is an anti-cancer agent or a further oncolytic virus.

Provided herein are methods of reducing growth of a cancer cell,exemplary methods comprising administering to the cancer cell aneffective amount of the recombinant oncolytic virus, the immunogeniccomposition, or the pharmaceutical composition according to anyembodiments as described herein.

Provided herein are methods of regressing the growth of a tumor,exemplary methods comprising administering to the tumor an effectiveamount of the recombinant oncolytic virus, the immunogenic composition,or the pharmaceutical composition according to any embodiments asdescribed herein. Further provided herein are methods, wherein the tumoris in a subject and the administering comprises administering to thesubject. Further provided herein are methods comprising administering afurther therapy, wherein the further therapy comprises chemotherapy,radiation, oncolytic viral therapy with an additional virus, treatmentwith immunomodulatory proteins, a CAR T cellular therapy, an anti-canceragent, or any combinations thereof. Further provided herein are methods,wherein the further therapy comprises administering an immunomodulatoryagent comprising anti-CD33 antibody and variable region thereof, ananti-CD11b antibody and variable region thereof, a COX2 inhibitor, acytokine, a chemokine, an anti-CTLA4 antibody or an antigen bindingfragment thereof, an anti-PD-1 antibody or an antigen binding fragmentthereof, an anti-PD-L1 antibody or an antigen binding fragment thereof,or a TLR agonist.

A method of treatment comprising administering to a subject in needthereof an effective amount of a recombinant oncolytic virus, theimmunogenic composition, or a pharmaceutical composition according toany embodiments described herein. Further provided herein are methods,wherein the administering comprises an intratumoral administration.Further provided herein are methods, wherein the administering comprisesa systemic administration. Further provided herein are methods, whereinthe systemic administration comprises at least one of: anintraperitoneal administration, an oral administration, an intravenousadministration, an intranasal administration, a sublingualadministration, a rectal administration, a transdermal administration,or any combination thereof. Further provided herein are methods, whereinthe subject has a cancer, and wherein the cancer is at least one of: amelanoma, a hepatocellular carcinoma, a breast cancer, a lung cancer, anon-small lung cancer, a peritoneal cancer, a prostate cancer, a bladdercancer, an ovarian cancer, a leukemia, a lymphoma, a renal cellcarcinoma, a pancreatic cancer, an epithelial carcinoma, a gastric/ GEjunction adenocarcinoma, a cervical cancer, a colon carcinoma, acolorectal cancer, a duodenal cancer, a pancreatic adenocarcinoma, anadenoid cystic, a sarcoma, a mesothelioma, a glioblastoma multiforme, anastrocytoma, a multiple myeloma, a prostate carcinoma, a hepatocellularcarcinoma, a cholangiocarcinoma, a head and neck squamous cellcarcinoma, a cervical squamous-cell carcinoma, an osteosarcoma, anepithelial ovarian carcinoma, an acute lymphoblastic lymphoma, amyeloproliferative neoplasm, or any combination thereof. Furtherprovided herein are methods, wherein the recombinant oncolytic virus,the immunogenic composition, or the pharmaceutical composition isadministered at a dosage that comprises from about 10⁶ PFU/mL to about10¹⁰ PFU/mL of the recombinant vaccinia virus. Further provided hereinare methods, wherein the recombinant oncolytic virus, or thepharmaceutical composition is administered at a dosage that comprisesabout 3 × 10⁹ PFU/mL of the recombinant vaccinia virus. Further providedherein are methods, wherein the recombinant oncolytic virus, theimmunogenic composition, or the pharmaceutical composition isadministered, independently, in an initial dose for a first period oftime, an intermediate dose for a second period of time, and a high dosefor a third period of time. Further provided herein are methods,comprising administration of the initial, the intermediate, and the highdose, independently, wherein the initial dose is lower than theintermediate dose and the intermediate dose is lower than the high dose.Further provided herein are methods, wherein the recombinant oncolyticvirus, the immunogenic composition, or the pharmaceutical composition isadministered, independently, in a high dose for a first period of time,an intermediate dose for a second period of time, and a low dose for athird period of time. Further provided herein are methods, comprisingadministration of the initial, the intermediate, and the low dose,independently, wherein the initial dose is higher than the intermediatedose and the intermediate dose is higher than the low dose. Furtherprovided herein are methods, wherein the first, second, and thirdperiods of time are each from about 1 day, about 2 days, about 3 days,about 4 days, about 5 days, about 6 days, about 1 week, about 2 week,about 3 weeks, about 4 weeks, about 6 weeks, about 7 weeks, about 8weeks, about 9 weeks, about 10, weeks, about 12 weeks, about 4 months,about 5 months, about 6 months, about 7 months, about 8 months, about 9months, about 10 months, about 11 months or about 1 year. Furtherprovided herein are methods, wherein the recombinant oncolytic virus,the immunogenic composition, or the pharmaceutical compositionindependently comprises a liquid dosage form that is administered at avolume of about 1 mL to about 5 mL, about 5 mL to 10 mL, about 15 mL toabout 20 mL, about 25 mL to about 30 mL, about 30 mL to about 50 mL,about 50 mL to about 100 mL, about 100 mL to 150 mL, about 150 mL toabout 200 mL, about 200 mL to about 250 mL, about 250 mL to about 300mL, about 300 mL to about 350 mL, about 350 mL to about 400 mL, about400 mL to about 450 mL, about 450 mL to 500 mL, about 500 mL to 750 mL,or about 750 mL to 1000 mL. Further provided herein are methods, whereinthe recombinant oncolytic virus, the immunogenic composition, or thepharmaceutical composition is administered in a liquid dosage form, asolid dosage form, an inhalable dosage form, an intranasal dosage form,a liposomal formulation, a dosage form comprising nanoparticles, adosage form comprising microparticles, a polymeric dosage form, or anycombination thereof. Further provided herein are methods, wherein therecombinant oncolytic virus, the immunogenic composition, or thepharmaceutical composition is administered for a duration of about 1day, about 2 days, about 3 days, about 4 days, about 5 days, about 6days, about 1 week, about 2 week, about 3 weeks, about 4 weeks, about 6weeks, about 7 weeks, about 8 weeks, about 9 weeks, about 10, weeks,about 12 weeks, about 4 months, about 5 months, about 6 months, about 7months, about 8 months, about 9 months, about 10 months, about 11months, or about 1 year. Further provided herein are methods, whereinthe recombinant oncolytic virus, the immunogenic composition, or thepharmaceutical composition is administered once daily, twice daily, onceevery week, once every two weeks, or once every three weeks. Furtherprovided herein are methods, wherein the recombinant oncolytic virus,the immunogenic composition, or the pharmaceutical composition isadministered as a bolus injection or a slow infusion. Further providedherein are methods, wherein the administration of the recombinantoncolytic virus, the immunogenic composition, or the pharmaceuticalcomposition results in a first peak viral load after about 1 hour toabout 3 days and a second peak viral load after about 3 days to about 10days from administration of a first dose. Further provided herein aremethods, comprising administration of a further therapy, wherein thefurther therapy is administered for a duration of about 1 day, about 2days, about 3 days, about 4 days, about 5 days, about 6 days, about 1week, about 2 week, about 3 weeks, about 4 weeks, about 6 weeks, about 7weeks, about 8 weeks, about 9 weeks, about 10, weeks, or about 12 weeks.Further provided herein are methods, wherein the further therapy isadministered once daily, twice daily, once every 1 day, once every 2days, once every 3 days, once every 4 days, once every 5 days, onceevery 6 days, once every 1 week, once every 2 week, once every 3 weeks,once every 4 weeks, once every 6 weeks, once every 7 weeks, once every 8weeks, once every 9 weeks, once every 10, weeks, once every 12 weeks,once every 4 months, once every 5 months, once every 6 months, onceevery 7 months, once every 8 months, once every 9 months, once every 10months, once every 11 months, or once every 1 year. Further providedherein are methods, wherein the further therapy is administered in aliquid dosage form, a solid dosage form, an inhalable dosage form, anintranasal dosage form, a liposomal formulation, a dosage formcomprising nanoparticles, a dosage form comprising microparticles, apolymeric dosage form, or any combination thereof. Further providedherein are methods, wherein the further therapy is administered in aliquid dosage form, a solid dosage form, an inhalable dosage form, anintranasal dosage form, a liposomal formulation, a dosage formcomprising nanoparticles, a dosage form comprising microparticles, apolymeric dosage form, or any combinations thereof. Further providedherein are methods, wherein the further therapy is administered orally,intravenously, by an intratumoral injection, by intraperitonealinjection, or by radiation. Further provided herein are methods, whereinthe further therapy comprises chemotherapy, radiation, oncolytic viraltherapy with an additional virus, treatment with immunomodulatoryproteins, a CAR T cellular therapy, an anti-cancer agent, or anycombinations thereof. Further provided herein are methods, wherein thefurther therapy comprises administration of an immunomodulatory agentcomprising anti-CD33 antibody and variable region thereof, an anti-CD11bantibody and variable region thereof, a COX2 inhibitor, a cytokine, achemokine, an anti-CTLA4 antibody or an antigen binding fragmentthereof, an anti-PD-1 antibody or an antigen binding fragment thereof,an anti-PD-L1 antibody or an antigen binding fragment thereof, or a TLRagonist. Further provided herein are methods, wherein the furthertherapy comprises administration of the anti-cancer agent, wherein theanti-cancer agent is a chemotherapeutic agent. Further provided hereinare methods, wherein the subject is human.

EXAMPLES

The examples below further illustrate the described embodiments withoutlimiting the scope of this disclosure.

Example 1: Tumor Model

Recombinant vaccinia virus was assayed in comparison to the same strainof virus without the modification as described herein in a tumor modelsystem. The below table lists the viruses for testing and themodifications in the viral genome for the same:

TABLE 1 MODEL Unique Identifier UID DESCRIPTION B16 Tumor Model WO0416NA52R- mut CXCR4 TK- WO0434N A52R- mut CXCR4 TK- 158- cpx012+ HCCTKM WR.TK- VFB Vehicle Formulated Buffer

Table 1 above shows that the viruses used in the study were recombinantvaccinia virus WO0434N (shown as A52R- mutCXCR4 TK- 158- cpx012+) andreference vaccinia virus WO0416N (A52R- mutCXCR4 TK-). The modificationto WO0434N was by deletion of TK gene and substitution of A52 gene withP7.5-driven mutant CXCR4 and substitution of A35 gene (WR158) withcowpox virus gene CPXV012. The reference vaccinia virus WO0416N had adeletion of TK gene and substitution of A52 gene with P7.5-driven mutantCXCR4. The controls were vaccinia virus Western Reserve Thymidine Kinasenegative (WR.TK-) strain (HCCTKM) and vehicle formulated buffer (VFB).The nucleic acid sequence of the P7.5 promoter is defined by SEQ IDNO: 1. The nucleic acid sequence of the mutant CXCR4 gene is defined bySEQ ID NO: 15. The nucleic acid sequence of the CPXV012 is defined bySEQ ID NO: 2. The study was performed in B16 tumor model. The tumorvolumes were measured 17 days after the virus administration for eachgroup and controls. The results as shown in FIG. 1 indicate anenhancement in the therapeutic activity with WO0434N virus as comparedto reference virus WO0416N or the controls HCCTKM and VFB.

Example 2: Strain Characterization

To assess whether a given virus is replication-competent orreplication-defective in a cell type, replication capacity is assessedof a recombinant vaccinia virus is assessed via PCR assay using serafrom a mammal or a rodent infected with the recombinant virus, a viralplaque assay, or any combinations thereof. For viral plaque assays,confluent monolayers of susceptible cells in tissue culture flasks areinfected with vaccinia virus. After incubation, cytopathic effects (CPE)are observed and visualized through formation of a halo or circularclearing the cell monolayer. Cell culture media is replaced with asolution that increases the viscosity. The replaced solution includesgelatin or carboxymethylcellulose. The viral plaque assays arevisualized by staining with an agent that increases cell contrast by eyeor by microscopy. Incubation following infection can be for 4 to 48hours before plaque can be observed. The staining agent is CrystalViolet. For PCR based assays, vaccinia virus content is quantified usingqPCR-based approaches.

Example 3: Tumor Growth Inhibition

Animal assays were performed in mouse models of cancer to assess tumorgrowth impact of compositions described herein. Briefly, modifiedvaccinia viruses were intratumorally injected (IT) to Renca and EMT6tumor bearing mice.

Modified vaccinia viruses were assessed in comparison to a VehicleFormulated Buffer (VFB). Group 1 was treated with a modified vacciniavirus comprising a TK gene deletion, insertion of nucleic acid encodingthe cowpox virus V012 protein (CPXV012) (SEQ ID NO: 2), a P7.5 promoter(SEQ ID NO: 1) and a loxP sequence (SEQ ID NO: 35). Group 2 was treatedwith a modified vaccinia virus comprising a WR158 gene deletion,insertion of nucleic acid encoding CPXV012 protein (SEQ ID NO: 2), aP7.5 promoter (SEQ ID NO: 1), and a loxP sequence (SEQ ID NO: 35). Group3 was treated with a vaccinia virus comprising a TK gene deletion andinsertion of nucleic acid encoding dominant negative interferonregulatory factor 7 (dnIRF7, SEQ ID NO: 36). Group 4 was treated with amodified vaccinia virus comprising a TK gene deletion and insertion ofnucleic acid encoding viral interferon regulator factor 3 (vIRF3, SEQ IDNO: 38).

Balb/c mice were implanted subcutaneously with RENCA cell or EMT6 celltumors. Mice were divided into groups of 10. Tumors were injected with asingle dose of 1×10⁷ pfu modified vaccinia virus or vehicle control.

Tumor volumes in mice with Renca tumors were measured after 23 days, asshown in FIG. 2A. Groups treated with virus expressing cowpox virus V012and vIRF3 showed the most effective reduction in Renca tumor volume.

Tumor volumes in mice with EMT6 tumors were measured after 27 days, asshown in FIG. 2B. Groups treated with virus expressing cowpox virus V012and dnIRF7 showed the most effective reduction in EMT6 tumor volume.

While preferred embodiments of the present invention have been shown anddescribed herein, it will be obvious to those skilled in the art thatsuch embodiments are provided by way of example only. Numerousvariations, changes, and substitutions will now occur to those skilledin the art without departing from the invention. It should be understoodthat various alternatives to the embodiments of the invention describedherein may be employed in practicing the invention. It is intended thatthe following claims define the scope of the invention and that methodsand structures within the scope of these claims and their equivalents becovered thereby.

TABLE 2 Sequences SEQ ID NO: PROTEIN/ NUCLEIC ACID NAME SEQUENCES 1 P7.5promoter (DNA) TCACTAATTCCAAACCCACCCGCTTTTTATAGTAAGTTTTTCACCCATAAATAATAAATACAATAATTAATTTCTCGTAAAAGTAGAAAATATATTCTAATTTATTGCACGGTAAGGAAGTAGATCATAA 2 CPXV012 (DNA)ATGTTCATCATGCGCGAGAGCATTTACCGCGTGATGATTGTCATTTTGTATTTGAGCTTGATTTCTTCGTTTTTGGTTATCTGCTCTATGGAGCACGGCTACTTCCAGGAGGGCATCAGCCGCTTCAAGATTTGTCCCTATCATTGGTATAAACAACACATGAGTTTATTGTTTCGTCGTTACTATCACAAGCTGGATAGTATCATCTAG 3 CPXV012 (polypeptide)MFIMRESIYRVMIVILYLSLISSFLVICSMEHGYFQEGISRFKICPYH WYKQHMSLLFRRYYHKLDSII 4HMGB1 (human, mutant, DNA) GGCAAAGGAGATCCTAAGAAGCCGAGAGGCAAAATGTCATCATATGCATTCTTCGTGCAAACTTGTCGGGAGGAGCATAAGAAGAAGCACCCAGATGCTGCAGTCAACTTCGCTGAGTTTGCAAAGAAGTGCGCTGAGAGGTGGAAGACCATGGCAGCTAAAGAGAAAGGAAAATTTGAAGATATGGCAAAAGCGGACAAGGCCCGTTATGAAAGAGAAATGAAAACCTATATCCCTCCCAAAGGGGAGACAAAAAAGAAGTTCAAGGACCCCAATGCACCCAAGAGGCCTCCTTCGGCCTTCTTCCTCTTCTGCTCTGAGTATCGCCCAAAAATCAAAGGAGAACATCCTGGCCTGTCCATTGGTGATGTTGCGAAGAAACTGGGAGAGATGTGGAATAACACTGCTGCAGATGACAAGCAGCCTTATGAAAAGAAGGCTGCGAAGCTGAAGGAAAAATATGAAAAGGATATTGCTGCATATCGAGCTAAAGGAAAGCCTGATGCAGCAAAAAAGGGAGTTGTCAAGGCTGAAAAAGCGAAGAAAAAGAAGGAAGAGGAGGAAGATGAGGAAGATGAAGAGGATGAGGAGGAGGAGGAAGATGAAGAAGATGAAGATGAAGAAGAAGATGATGATGATGAATAA 5 HMGB1 (human, mutant, protein)GKGDPKKPRGKMSSYAFFVQTCREEHKKKHPDAAVNFAEFAKKCAERWKTMAAKEKGKFEDMAKADKARYEREMKTYIPPKGETKKKFKDPNAPKRPPSAFFLFCSEYRPKIKGEHPGLSIGDVAKKLGEMWNNTAADDKQPYEKKAAKLKEKYEKDIAAYRAKGKPDAAKKGVVKAEKAKKKKEEEEDEEDEEDEEEEEDEEDEDEEEDDDDE 6 IgE derived signal sequence (DNA)ATGGACTGGACATGGATTCTCTTTCTAGTGGCCGCAGCCACAAG GGTCCACTCC 7 IgE derivedsignal sequence (polypeptide) MDWTWILFLVAAATRVHS 8 HMGB1 withIgE-derived signal sequence (human, mutant, DNA)ATGGACTGGACATGGATTCTCTTTCTAGTGGCCGCAGCCACAAGGGTCCACTCCGGCAAAGGAGATCCTAAGAAGCCGAGAGGCAAAATGTCATCATATGCATTCTTCGTGCAAACTTGTCGGGAGGAGCATAAGAAGAAGCACCCAGATGCTGCAGTCAACTTCGCTGAGTTTGCAAAGAAGTGCGCTGAGAGGTGGAAGACCATGGCAGCTAAAGAGAAAGGAAAATTTGAAGATATGGCAAAAGCGGACAAGGCCCGTTATGAAAGAGAAATGAAAACCTATATCCCTCCCAAAGGGGAGACAAAAAAGAAGTTCAAGGACCCCAATGCACCCAAGAGGCCTCCTTCGGCCTTCTTCCTCTTCTGCTCTGAGTATCGCCCAAAAATCAAAGGAGAACATCCTGGCCTGTCCATTGGTGATGTTGCGAAGAAACTGGGAGAGATGTGGAATAACACTGCTGCAGATGACAAGCAGCCTTATGAAAAGAAGGCTGCGAAGCTGAAGGAAAAATATGAAAAGGATATTGCTGCATATCGAGCTAAAGGAAAGCCTGATGCAGCAAAAAAGGGAGTTGTCAAGGCTGAAAAAGCGAAGAAAAAGAAGGAAGAGGAGGAAGATGAGGAAGATGAAGAGGATGAGGAGGAGGAGGAAGATGAAGAAGATGAAGATGAAGAAGAAGATGATGATGATGAAT AA 9 HMGB1 with IgE-derivedsignal sequence (human, mutant, polypeptide)MDWTWILFLVAAATRVHSGKGDPKKPRGKMSSYAFFVQTCREEHKKKHPDAAVNFAEFAKKCAERWKTMAAKEKGKFEDMAKADKARYEREMKTYIPPKGETKKKFKDPNAPKRPPSAFFLFCSEYRPKIKGEHPGLSIGDVAKKLGEMWNNTAADDKQPYEKKAAKLKEKYEKDIAAYRAKGKPDAAKKGVVKAEKAKKKKEEEEDEEDEEDEEEEEDEEDE DEEEDDDDE 10 IL15 (human,polypeptide) MRISKPHLRSISIQCYLCLLLNSHFLTEAGIHVFILGCFSAGLPKTEANWVNVISDLKKIEDLIQSMHIDATLYTESDVHPSCKVTAMKCFLLELQVISLESGDASIHDTVENLIILANNSLSSNGNVTESGCKECEELEEKNIK EFLQSFVHIVQMFINTS 11IL-7 (mouse, DNA) ATGTTCCATGTTTCTTTTAGATATATCTTTGGAATTCCTCCACTGATCCTTGTTCTGCTGCCTGTCACATCATCTGAGTGCCACATTAAAGACAAAGAAGGTAAAGCATATGAGAGTGTACTGATGATCAGCATCGATGAATTGGACAAAATGACAGGAACTGATAGTAATTGCCCGAATAATGAACCAAACTTTTTTAGAAAACATGTATGTGATGATACAAAGGAAGCTGCTTTTCTAAATCGTGCTGCTCGCAAGTTGAAGCAATTTCTTAAAATGAATATCAGTGAAGAATTCAATGTCCACTTACTAACAGTATCACAAGGCACACAAACACTGGTGAACTGCACAAGTAAGGAAGAAAAAAACGTAAAGGAACAGAAAAAGAATGATGCATGTTTCCTAAAGAGACTACTGAGAGAAATAAAAACTTGTTGGAATAA AATTTTGAAGGGCAGTATATAA 12IL-7 (human, DNA) ATGTTCCATGTTTCTTTTAGGTATATCTTTGGACTTCCTCCCCTGATCCTTGTTCTGTTGCCAGTAGCATCATCTGATTGTGATATTGAAGGTAAAGATGGCAAACAATATGAGAGTGTTCTAATGGTCAGCATCGATCAATTATTGGACAGCATGAAAGAAATTGGTAGCAATTGCCTGAATAATGAATTTAACTTTTTTAAAAGACATATCTGTGATGCTAATAAGGAAGGTATGTTTTTATTCCGTGCTGCTCGCAAGTTGAGGCAATTTCTTAAAATGAATAGCACTGGTGATTTTGATCTCCACTTATTAAAAGTTTCAGAAGGCACAACAATACTGTTGAACTGCACTGGCCAGGTTAAAGGAAGAAAACCAGCTGCCCTGGGTGAAGCCCAACCAACAAAGAGTTTGGAAGAAAATAAATCTTTAAAGGAACAGAAAAAACTGAATGACTTGTGTTTCCTAAAGAGACTATTACAAGAGATAAAAACTTGTTGGAATAAAATTTTGATGGGCACTAAAGAACACT GA 13 IL-7 (mouse, protein)MFHVSFRYIFGIPPLILVLLPVTSSECHIKDKEGKAYESVLMISIDELDKMTGTDSNCPNNEPNFFRKHVCDDTKEAAFLNRAARKLKQFLKMNISEEFNVHLLTVSQGTQTLVNCTSKEEKNVKEQKKNDACFLKRLLR EIKTCWNKILKGSI 14 IL-7(human, protein) MFHVSFRYIFGLPPLILVLLPVASSDCDIEGKDGKQYESVLMVSIDQLLDSMKEIGSNCLNNEFNFFKRHICDANKEGMFLFRAARKLRQFLKMNSTGDFDLHLLKVSEGTTILLNCTGQVKGRKPAALGEAQPTKSLEENKSLKEQKKLNDLCFLKRLLQEIKTCWNKILMGTKEH 15 CXCR4 (Y157A, human, DNA)ATGGAGGGGATCAGTATATACACTTCAGATAACTACACCGAGGAAATGGGCTCAGGGGACTATGACTCCATGAAGGAACCCTGTTTCCGTGAAGAAAATGCTAATTTCAATAAAATCTTCCTGCCCACCATCTACTCCATCATCTTCTTAACTGGCATTGTGGGCAATGGATTGGTCATCCTGGTCATGGGTTACCAGAAGAAACTGAGAAGCATGACGGACAAGTACAGGCTGCACCTGTCAGTGGCCGACCTCCTCTTTGTCATCACGCTTCCCTTCTGGGCAGTTGATGCCGTGGCAAACTGGTACTTTGGGAACTTCCTATGCAAGGCAGTCCATGTCATCTACACAGTCAACCTCTACAGCAGTGTCCTCATCCTGGCCTTCATCAGTCTGGACCGCTACCTGGCCATCGTCCACGCCACCAACAGTCAGAGGCCAAGGAAGCTGTTGGCTGAAAAGGTGGTCGCTGTTGGCGTCTGGATCCCTGCCCTCCTGCTGACTATTCCCGACTTCATCTTTGCCAACGTCAGTGAGGCAGATGACAGATATATCTGTGACCGCTTCTACCCCAATGACTTGTGGGTGGTTGTGTTCCAGTTTCAGCACATCATGGTTGGCCTTATCCTGCCTGGTATTGTCATCCTGTCCTGCTATTGCATTATCATCTCCAAGCTGTCACACTCCAAGGGCCACCAGAAGCGCAAGGCCCTCAAGACCACAGTCATCCTCATCCTGGCTTTCTTCGCCTGTTGGCTGCCTTACTACATTGGGATCAGCATCGACTCCTTCATCCTCCTGGAAATCATCAAGCAAGGGTGTGAGTTTGAGAACACTGTGCACAAGTGGATTTCCATCACCGAGGCCCTAGCTTTCTTCCACTGTTGTCTGAACCCCATCCTCTATGCTTTCCTTGGAGCCAAATTTAAAACCTCTGCCCAGCACGCACTCACCTCTGTGAGCAGAGGGTCCAGCCTCAAGATCCTCTCCAAAGGAAAGCGAGGTGGACATTCATCTGTTTCCACTGAGTCTGAGTCTTCAAGTTTTCACTCCAGCTAA 16 CXCR4 (Y159A, mouse, DNA)ATGGAACCGATCAGTGTGAGTATATACACTTCTGATAACTACTCTGAAGAAGTGGGTTCTGGAGACTATGACTCCAACAAGGAACCCTGCTTCCGGGATGAAAACGTCCATTTCAATAGGATCTTCCTGCCCACCATCTACTTCATCATCTTCTTGACTGGCATAGTCGGCAATGGATTGGTGATCCTGGTCATGGGTTACCAGAAGAAGCTAAGGAGCATGACGGACAAGTACCGGCTGCACCTGTCAGTGGCTGACCTCCTCTTTGTCATCACACTCCCCTTCTGGGCAGTTGATGCCATGGCTGACTGGTACTTTGGGAAATTTTTGTGTAAGGCTGTCCATATCATCTACACTGTCAACCTCTACAGCAGCGTTCTCATCCTGGCCTTCATCAGCCTGGACCGATACCTCGCTATTGTCCACGCCACCAACAGTCAGAGGCCAAGGAAACTGCTGGCTGAAAAGGCAGTCGCTGTGGGCGTCTGGATCCCAGCCCTCCTCCTGACTATACCTGACTTCATCTTTGCCGACGTCAGCCAGGGGGACATCAGTCAGGGGGATGACAGGTACATCTGTGACCGCCTTTACCCCGATAGCCTGTGGATGGTGGTGTTTCAATTCCAGCATATAATGGTGGGTCTCGTCCTGCCCGGCATCGTCATCCTCTCCTGTTACTGCATCATCATCTCTAAGCTGTCACACTCCAAGGGCCACCAGAAGCGCAAGGCCCTCAAGACGACAGTCATCCTCATCCTAGCTTTCTTTGCCTGCTGGCTGCCATATTATGTGGGGATCAGCATCGACTCCTTCATCCTTTTGGGGGTCATCAAGCAAGGATGTGACTTCGAGAGCATCGTGCACAAGTGGATCTCCATCACAGAGGCCCTCGCCTTCTTCCACTGTTGCCTGAACCCCATCCTCTATGCCTTCCTCGGGGCCAAGTTCAAAAGCTCTGCCCAGCATGCACTCAACTCCATGAGCAGAGGCTCCAGCCTCAAGATCCTTTCCAAAGGAAAGCGGGGTGGACACTCTTCCGTCTCCACGGAGTCAGAATCCTCCAGTTTTCACT CCAGCTAA 17 CXCR4(wild-type, human, DNA) ATGGAGGGGATCAGTATATACACTTCAGATAACTACACCGAGGAAATGGGCTCAGGGGACTATGACTCCATGAAGGAACCCTGTTTCCGTGAAGAAAATGCTAATTTCAATAAAATCTTCCTGCCCACCATCTACTCCATCATCTTCTTAACTGGCATTGTGGGCAATGGATTGGTCATCCTGGTCATGGGTTACCAGAAGAAACTGAGAAGCATGACGGACAAGTACAGGCTGCACCTGTCAGTGGCCGACCTCCTCTTTGTCATCACGCTTCCCTTCTGGGCAGTTGATGCCGTGGCAAACTGGTACTTTGGGAACTTCCTATGCAAGGCAGTCCATGTCATCTACACAGTCAACCTCTACAGCAGTGTCCTCATCCTGGCCTTCATCAGTCTGGACCGCTACCTGGCCATCGTCCACGCCACCAACAGTCAGAGGCCAAGGAAGCTGTTGGCTGAAAAGGTGGTCTATGTTGGCGTCTGGATCCCTGCCCTCCTGCTGACTATTCCCGACTTCATCTTTGCCAACGTCAGTGAGGCAGATGACAGATATATCTGTGACCGCTTCTACCCCAATGACTTGTGGGTGGTTGTGTTCCAGTTTCAGCACATCATGGTTGGCCTTATCCTGCCTGGTATTGTCATCCTGTCCTGCTATTGCATTATCATCTCCAAGCTGTCACACTCCAAGGGCCACCAGAAGCGCAAGGCCCTCAAGACCACAGTCATCCTCATCCTGGCTTTCTTCGCCTGTTGGCTGCCTTACTACATTGGGATCAGCATCGACTCCTTCATCCTCCTGGAAATCATCAAGCAAGGGTGTGAGTTTGAGAACACTGTGCACAAGTGGATTTCCATCACCGAGGCCCTAGCTTTCTTCCACTGTTGTCTGAACCCCATCCTCTATGCTTTCCTTGGAGCCAAATTTAAAACCTCTGCCCAGCACGCACTCACCTCTGTGAGCAGAGGGTCCAGCCTCAAGATCCTCTCCAAAGGAAAGCGAGGTGGACATTCATCTGTTTCCACTGAGTCTGAGTCTTCAAGTTTTCACTCCAGCTAA 18 CXCR4 (Y157A, human) (polypeptide)MEGISIYTSDNYTEEMGSGDYDSMKEPCFREENANFNKIFLPTIYSIIFLTGIVGNGLVILVMGYQKKLRSMTDKYRLHLSVADLLFVITLPFWAVDAVANWYFGNFLCKAVHVIYTVNLYSSVLILAFISLDRYLAIVHATNSQRPRKLLAEKVVAVGVWIPALLLTIPDFIFANVSEADDRYICDRFYPNDLWVVVFQFQHIMVGLILPGIVILSCYCIIISKLSHSKGHQKRKALKTTVILILAFFACWLPYYIGISIDSFILLEIIKQGCEFENTVHKWISITEALAFFHCCLNPILYAFLGAKFKTSAQHALTSVSRGSSLKILSKGKR GGHSSVSTESESSSFHSS 19CXCR4 (Y159A, mouse) (polypeptide)MEPISVSIYTSDNYSEEVGSGDYDSNKEPCFRDENVHFNRIFLPTIYFIIFLTGIVGNGLVILVMGYQKKLRSMTDKYRLHLSVADLLFVITLPFWAVDAMADWYFGKFLCKAVHIIYTVNLYSSVLILAFISLDRYLAIVHATNSQRPRKLLAEKAVAVGVWIPALLLTIPDFIFADVSQGDISQGDDRYICDRLYPDSLWMVVFQFQHIMVGLVLPGIVILSCYCIIISKLSHSKGHQKRKALKTTVILILAFFACWLPYYVGISIDSFILLGVIKQGCDFESIV HKWISITEALAFFHCCLNPILYAFLGAKFKSSAQHALNSMSRGSSLKI LSKGKRGGHSSVSTESESSSFHSS 20 CXCR4 (wild-type,human, polypeptide) MEGISIYTSDNYTEEMGSGDYDSMKEPCFREENANFNKIFLPTIYSIIFLTGIVGNGLVILVMGYQKKLRSMTDKYRLHLSVADLLFVITLPFWAVDAVANWYFGNFLCKAVHVIYTVNLYSSVLILAFISLDRYLAIVHATNSQRPRKLLAEKVVYVGVWIPALLLTIPDFIFANVSEADDRYICDRFYPNDLWVVVFQFQHIMVGLILPGIVILSCYCIIISKLSHSKGHQKRKALKTTVILILAFFACWLPYYIGISIDSFILLEIIKQGCEFENTVHKWISITEALAFFHCCLNPILYAFLGAKFKTSAQHALTSVSRGSSLKILSKGKR GGHSSVSTESESSSFHSS 21CCR2 (Human, DNA) ATGCTGTCCACATCTCGTTCTCGGTTTATCAGAAATACCAACGAGAGCGGTGAAGAAGTCACCACCTTTTTTGATTATGATTACGGTGCTCCCTGTCATAAATTTGACGTGAAGCAAATTGGGGCCCAACTCCTGCCTCCGCTCTACTCGCTGGTGTTCATCTTTGGTTTTGTGGGCAACATGCTGGTCGTCCTCATCTTAATAAACTGCAAAAAGCTGAAGTGCTTGACTGACATTTACCTGCTCAACCTGGCCATCTCTGATCTGCTTTTTCTTATTACTCTCCCATTGTGGGCTCACTCTGCTGCAAATGAGTGGGTCTTTGGGAATGCAATGTGCAAATTATTCACAGGGCTGTATCACATCGGTTATTTTGGCGGAATCTTCTTCATCATCCTCCTGACAATCGATAGATACCTGGCTATTGTCCATGCTGTGTTTGCTTTAAAAGCCAGGACGGTCACCTTTGGGGTGGTGACAAGTGTGATCACCTGGTTGGTGGCTGTGTTTGCTTCTGTCCCAGGAATCATCTTTACTAAATGCCAGAAAGAAGATTCTGTTTATGTCTGTGGCCCTTATTTTCCACGAGGATGGAATAATTTCCACACAATAATGAGGAACATTTTGGGGCTGGTCCTGCCGCTGCTCATCATGGTCATCTGCTACTCGGGAATCCTGAAAACCCTGCTTCGGTGTCGAAACGAGAAGAAGAGGCATAGGGCAGTGAGAGTCATCTTCACCATCATGATTGTTTACTTTCTCTTCTGGACTCCCTATAATATTGTCATTCTCCTGAACACCTTCCAGGAATTCTTCGGCCTGAGTAACTGTGAAAGCACCAGTCAACTGGACCAAGCCACGCAGGTGACAGAGACTCTTGGGATGACTCACTGCTGCATCAATCCCATCATCTATGCCTTCGTTGGGGAGAAGTTCAGAAGCCTTTTTCACATAGCTCTTGGCTGTAGGATTGCCCCACTCCAAAAACCAGTGTGTGGAGGTCCAGGAGTGAGACCAGGAAAGAATGTGAAAGTGACTACACAAGGACTCCTCGATGGTCGTGGAAAAGGAAAGTCAATTGGCAGAGCCCCTGAAGCCAGTCTTCAGGACAAAGA AGGAGCCTAG 22 CCR2 (Mouse,DNA) ATGGAAGACAATAATATGTTACCTCAGTTCATCCACGGCATACTATCAACATCTCATTCTCTATTTACACGAAGTATCCAAGAGCTTGATGAAGGGGCCACCACACCGTATGACTACGATGATGGTGAGCCTTGTCATAAAACCAGTGTGAAGCAAATTGGAGCTTGGATCCTGCCTCCACTCTACTCCCTGGTATTCATCTTTGGTTTTGTGGGCAACATGTTGGTCATTATAATTCTGATAGGCTGTAAAAAGCTGAAGAGCATGACTGATATCTATCTGCTCAACTTGGCCATCTCTGACCTGCTCTTCCTGCTCACATTACCATTCTGGGCTCACTATGCTGCAAATGAGTGGGTCTTTGGGAATATAATGTGTAAAGTATTCACAGGGCTCTATCACATTGGTTATTTTGGTGGAATCTTTTTCATTATCCTCCTGACAATTGATAGGTACTTGGCTATTGTTCATGCTGTGTTTGCTTTAAAAGCCAGGACAGTTACCTTTGGGGTGATAACAAGTGTAGTCACTTGGGTGGTGGCTGTGTTTGCCTCTCTACCAGGAATCATATTTACTAAATCCAAACAAGATGATCACCATTACACCTGTGGCCCTTATTTTACACAACTATGGAAGAATTTCCAAACAATAATGAGAAATATCTTGAGCCTGATCCTGCCTCTACTTGTCATGGTCATCTGCTACTCAGGAATTCTCCACACCCTGTTTCGCTGTAGGAATGAGAAGAAGAGGCACAGGGCTGTGAGGCTCATCTTTGCCATCATGATTGTCTACTTTCTCTTCTGGACTCCATACAATATTGTTCTCTTCTTGACCACCTTCCAGGAATCCTTGGGAATGAGTAACTGTGTGATTGACAAGCACTTAGACCAGGCCATGCAGGTGACAGAGACTCTTGGAATGACACACTGCTGCATTAATCCTGTCATTTATGCCTTTGTTGGAGAGAAGTTCCGAAGGTATCTCTCCATATTTTTCAGAAAGCACATTGCTAAACGTCTCTGCAAACAGTGCCCAGTTTTCTATAGGGAGACAGCAGATCGAGTAAGCTCTACATTCACTCCTTCCACTGGGGAGCAAGAGGTCTCGGTTGGGT TGTAA 23 CCR2 (Human,protein) MLSTSRSRFIRNTNESGEEVTTFFDYDYGAPCHKFDVKQIGAQLLPPLYSLVFIFGFVGNMLVVLILINCKKLKCLTDIYLLNLAISDLLFLITLPLWAHSAANEWVFGNAMCKLFTGLYHIGYFGGIFFIILLTIDRYLAIVHAVFALKARTVTFGVVTSVITWLVAVFASVPGIIFTKCQKEDSVYVCGPYFPRGWNNFHTIMRNILGLVLPLLIMVICYSGILKTLLRCRNEKKRHRAVRVIFTIMIVYFLFWTPYNIVILLNTFQEFFGLSNCESTSQLDQATQVTETLGMTHCCINPIIYAFVGEKFRSLFHIALGCRIAPLQKPVCGGPGVRPGKNVKVTTQGLLDGRGKGKSIGRAPEASLQDKEGA 24 CCR2 (Mouse, protein)MEDNNMLPQFIHGILSTSHSLFTRSIQELDEGATTPYDYDDGEPCHKTSVKQIGAWILPPLYSLVFIFGFVGNMLVIIILIGCKKLKSMTDIYLLNLAISDLLFLLTLPFWAHYAANEWVFGNIMCKVFTGLYHIGYFGGIFFIILLTIDRYLAIVHAVFALKARTVTFGVITSVVTWVVAVFASLPGIIFTKSKQDDHHYTCGPYFTQLWKNFQTIMRNILSLILPLLVMVICYSGILHTLFRCRNEKKRHRAVRLIFAIMIVYFLFWTPYNIVLFLTTFQESLGMSNCVIDKHLDQAMQVTETLGMTHCCINPVIYAFVGEKFRRYLSIFFRKHIAKRLCKQCPVFYRETADRVSSTFTPSTGEQEVSVGL 25 PH-20 (human, full-length)(DNA) ATGGGAGTGCTAAAATTCAAGCACATCTTTTTCAGAAGCTTTGTTAAATCAAGTGGAGTATCCCAGATAGTTTTCACCTTCCTTCTGATTCCATGTTGCTTGACTCTGAATTTCAGAGCACCTCCTGTTATTCCAAATGTGCCTTTCCTCTGGGCCTGGAATGCCCCAAGTGAATTTTGTCTTGGAAAATTTGATGAGCCACTAGATATGAGCCTCTTCTCTTTCATAGGAAGCCCCCGAATAAACGCCACCGGGCAAGGTGTTACAATATTTTATGTTGATAGACTTGGCTACTATCCTTACATAGATTCAATCACAGGAGTAACTGTGAATGGAGGAATCCCCCAGAAGATTTCCTTACAAGACCATCTGGACAAAGCTAAGAAAGACATTACATTTTATATGCCAGTAGACAATTTGGGAATGGCTGTTATTGACTGGGAAGAATGGAGACCCACTTGGGCAAGAAACTGGAAACCTAAAGATGTTTACAAGAATAGGTCTATTGAATTGGTTCAGCAACAAAATGTACAACTTAGTCTCACAGAGGCCACTGAGAAAGCAAAACAAGAATTTGAAAAGGCAGGGAAGGATTTCCTGGTAGAGACTATAAAATTGGGAAAATTACTTCGGCCAAATCACTTGTGGGGTTATTATCTTTTTCCGGATTGTTACAACCATCACTATAAGAAACCCGGTTACAATGGAAGTTGCTTCAATGTAGAAATAAAAAGAAATGATGATCTCAGCTGGTTGTGGAATGAAAGCACTGCTCTTTACCCATCCATTTATTTGAACACTCAGCAGTCTCCTGTAGCTGCTACACTCTATGTGCGCAATCGAGTTCGGGAAGCCATCAGAGTTTCCAAAATACCTGATGCAAAAAGTCCACTTCCGGTTTTTGCATATACCCGCATAGTTTTTACTGATCAAGTTTTGAAATTCCTTTCTCAAGATGAACTTGTGTATACATTTGGCGAAACTGTTGCTCTGGGTGCTTCTGGAATTGTAATATGGGGAACCCTCAGTATAATGCGAAGTATGAAATCTTGCTTGCTCCTAGACAATTACATGGAGACTATACTGAATCCTTACATAATCAACGTCACACTAGCAGCCAAAATGTGTAGCCAAGTGCTTTGCCAGGAGCAAGGAGTGTGTATAAGGAAAAACTGGAATTCAAGTGACTATCTTCACCTCAACCCAGATAATTTTGCTATTCAACTTGAGAAAGGTGGAAAGTTCACAGTACGTGGAAAACCGACACTTGAAGACCTGGAGCAATTTTCTGAAAAATTTTATTGCAGCTGTTATAGCACCTTGAGTTGTAAGGAGAAAGCTGATGTAAAAGACACTGATGCTGTTGATGTGTGTATTGCTGATGGTGTCTGTATAGATGCTTTTCTAAAACCTCCCATGGAGACAGAAGAACCTCAAATTTTCTACAATGCTTCACCCTCCACACTATCTGCCACAATGTTCATTGTTAGTATTTTGTTTCTTATCATTTCTT CTGTAGCGAGTTTGTAA 26PH-20 (human, full-length) (protein)MGVLKFKHIFFRSFVKSSGVSQIVFTFLLIPCCLTLNFRAPPVIPNVPFLWAWNAPSEFCLGKFDEPLDMSLFSFIGSPRINATGQGVTIFYVDRLGYYPYIDSITGVTVNGGIPQKISLQDHLDKAKKDITFYMPVDNLGMAVIDWEEWRPTWARNWKPKDVYKNRSIELVQQQNVQLSLTEATEKAKQEFEKAGKDFLVETIKLGKLLRPNHLWGYYLFPDCYNHHYKKPGYNGSCFNVEIKRNDDLSWLWNESTALYPSIYLNTQQSPVAATLYVRNRVREAIRVSKIPDAKSPLPVFAYTRIVFTDQVLKFLSQDELVYTFGETVALGASGIVIWGTLSIMRSMKSCLLLDNYMETILNPYIINVTLAAKMCSQVLCQEQGVCIRKNWNSSDYLHLNPDNFAIQLEKGGKFTVRGKPTLEDLEQFSEKFYCSCYSTLSCKEKADVKDTDAVDVCIADGVCIDAFLKPPMETEEPQIFYNASPSTLSATMFIVSILFLIISSVASL 27 Hyaluronidase (DNA)CCGCGATACGAATGTTCAAACGCCAGATTATGAAAAGTTGAGGAACACATGGCTGAACGTTAACTACGGTTATGATCAGTATGATGAGAAGAATGACGCAATGAAGAAGAAGTTTGATGCTACGGAGAAAGAGGCAGAGAAATTACTCAGTAGCATGAAAACTGAAAGTGGAAGGACTTACTTGTGGGATAGTGCAAAAGATTTAGATAACAAGTCTGCGGATATGACTCGTACCTATCGTAATATTGAGAAAATCGCAGAAGCGATGAAGCATAAAGATACTAAGTTAAATACTCCGGATAATAAAAACAAAGTTAAAGATGCCCTTGAGTGGCTGCATAAAAATGCCTATGGAAAAGAACCGGTGAAAAAACTTGAAGAACTAAAAACAAATTTCTCAAAATCAGCACCTCAAAAGAATACAAACTTAAATTGGTGGGATTATGAAATTGGAACACCTAGAGCACTAACAAATACCCTTATACTCTTAAAAGAAGATTTTACTGATGAAGAAAAGAAAAAATACACTGCCCCTATTAAAACTTTCGCCCCAAAAAGTGATGAAATATTATCTTCTGTAGGAAAAGCTGAACCTGCTAAAGGCGGAAATTTAGTAGACATTTCTAAAGTAAAACTTTTAGAAAGTATTATCGAAGAAGATGCAACTATGATGAAAGAATCAATAGAGGCATTTAATAAAGTCTTCACTTACGTTCAAAGTAATGCAACTGGTAAAGAACGTAATGGATTCTATAAAGACGGCTCTTATATTGATCATCAAGACGTCCCATACACTGGTGCTTATGGCGTTGTACTCTTAGAGGGGATTTCTCAAATGATGCCGATGATAAAAGAAACACCTTTTAAAGATAGTAATCAAAATGATACAACATTAAAGTCGTGGATTGATGAAGGATTTATGCCACTCATTTATAAAGGTGAAATGATGGATTTATCACGTGGTAGAGCCATTAGCCGTGAAAATGAAACGAGTCACTCAACATCTGCAACTGTAATGAAATCATTGTTGAGATTAAGTGATGCCATGGATGAGTCAACAAAAGCTAAATATAAGCAAATCGTTAAAACTTCTGTTAAATCTGATTCAAGTTATAAACAAAACGATTATTTAAGCTCTTATTCAGATATAAGCAAAATGAAGTCTTTAATTGAAGACAGCACTATTTCTACTAACGGTTTAACACAACAACTTAAAATATATAATGACATGAATCGTGTCACCTATCATAACAAAGACTTAGACTTTGCATTTGGCTTAAGTATGACGTCGAAAAACGTCGCACATTACGAAAGTATCAACGGAGAGAACTTAAAAGGTTGGCACACTGGTGCTGGAATGTCTTATTTATACAATAGCGATGTGAAACACTACCGTGATAACTTCTGGGCGACAGCTGATATGAAACGTTTAGCAGGTACTACAACTTTAGATAATGAAGAACCTAAAGAAAATAAGAACTCCGATAAAACTTTTGTAGGCGGAACAAAATTCGATGACCAACATGCTAGTATCGGAATGGATTTTGAAAATCAGGACAAAACTTTAACTGCCAAAAAATCATATTTCATATTAAACGATAAAATTGTCTTCTTAGGAACTGGCATTAAAAGTACTGATTCATCAAAGAATCCAGTGACAACGATTGAAAATCGCAAATCGAATGGGTATACGTTATTTACAGACGATAAACAAACAACCGCTTCAAATATTAATGATCAGGAAACCAATTCAGTCTTTTTAGAGTCCACAGATACAAAAAAGAACATCGGTTATCATTTTTTAAACGAATCGAAAATAACTGTAAAAAAAGAAAGTCATACTGGTAAGTGGAGTGATATAAATAAAAGTCAAAAGTCAGATGACAAAACTGATGAGTATTATGAAGTAACTCAAAAGCATTCTAATACAGATGATAAATATGCATATGTCTTGTATCCAGGCTTATCTAAAGATAATTTTAAATCCAAAGCAAGCCAAGTAACTATCGTTAAACAAGATGATGACTTCCACATTGTGAAAGATAATGAATCGGTTTGGGCTGGTGTCAATTATAGTAATAGCACTCAAACTTTTGACATTAACAACACCAAGGTTGAGGTTAAAGCGAAAGGGATGTTCATTTTGAAAAACAAGGACGATAATACGTACGAATGCTCATTCTATAATCCTGAGTCTACGAATACGGCTTCAGACATAGAAAGTAAGATCAGTATGACGGGATACTCAATCACGAATAAAAACACAAGTACGTCCAACGAAAGTGGTGTGCATTTCGAGTTGACTAAATATGCTGCCGCGATGTCTGGAGCAGGTCCGTGGGCAGCCTGGCCATTCCTACTCTCACTGGCGCTCATGCTACT ATGGCTGCTCTCATGA 28Hyaluronidase (protein) GRDTNVQTPDYEKLRNTWLNVNYGYDQTDEKNDAMKKKFDATEKEAEKLLSSMKTESGRTYLWDSAKDLDNKSADMTRTYRNIEKIAEAMKHKDTKLNTPDNKNKVKDALEWLHKNAYGKEPVKKLEELKTNFSKSAPQKNTNLNWWDYEIGTPRALTNTLILLKEDFTDEEKKKYTAPIKTFAPKSDEILSSVGKAEPAKGGNLVDISKVKLLESIIEEDATMMKESIEAFNKVFTYVQSNATGKERNGFYKDGSYIDHQDVPYTGAYGVVLLEGISQMMPMIKETPFKDSNQNDTTLKSWIDEGFMPLIYKGEMMDLSRGRAISRENETSHSTSATVMKSLLRLSDAMDESTKAKYKQIVKTSVKSDSSYKQNDYLSSYSDISKMKSLIEDSTISTNGLTQQLKIYNDMNRVTYHNKDLDFAFGLSMTSKNVAHYESINGENLKGWHTGAGMSYLYNSDVKHYRDNFWATADMKRLAGTTTLDNEEPKENKNSDKTFVGGTKFDDQHASIGMDFENQDKTLTAKKSYFILNDKIVFLGTGIKSTDSSKNPVTTIENRKSNGYTLFTDDKQTTASNINDQETNSVFLESTDTKKNIGYHFLNESKITVKKESHTGKWSDINKSQKSDDKTDEYYEVTQKHSNTDDKYAYVLYPGLSKDNFKSKASQVTIVKQDDDFHIVKDNESVWAGVNYSNSTQTFDINNTKVEVKAKGMFILKNKDDNTYECSFYNPESTNTASDIESKISMTGYSITNKNTSTSNESGVHFELTKYAAAM SGAGPWAAWPFLLSLALMLLWLLS29 Hyaluronidase with IgE-derived signal sequence (DNA)ATGGACTGGACATGGATTCTCTTTCTAGTGGCCGCAGCCACAAGGGTCCACAGCGGCCGCGATACGAATGTTCAAACGCCAGATTATGAAAAGTTGAGGAACACATGGCTGAACGTTAACTACGGTTATGATCAGTATGATGAGAAGAATGACGCAATGAAGAAGAAGTTTGATGCTACGGAGAAAGAGGCAGAGAAATTACTCAGTAGCATGAAAACTGAAAGTGGAAGGACTTACTTGTGGGATAGTGCAAAAGATTTAGATAACAAGTCTGCGGATATGACTCGTACCTATCGTAATATTGAGAAAATCGCAGAAGCGATGAAGCATAAAGATACTAAGTTAAATACTCCGGATAATAAAAACAAAGTTAAAGATGCCCTTGAGTGGCTGCATAAAAATGCCTATGGAAAAGAACCGGTGAAAAAACTTGAAGAACTAAAAACAAATTTCTCAAAATCAGCACCTCAAAAGAATACAAACTTAAATTGGTGGGATTATGAAATTGGAACACCTAGAGCACTAACAAATACCCTTATACTCTTAAAAGAAGATTTTACTGATGAAGAAAAGAAAAAATACACTGCCCCTATTAAAACTTTCGCCCCAAAAAGTGATGAAATATTATCTTCTGTAGGAAAAGCTGAACCTGCTAAAGGCGGAAATTTAGTAGACATTTCTAAAGTAAAACTTTTAGAAAGTATTATCGAAGAAGATGCAACTATGATGAAAGAATCAATAGAGGCATTTAATAAAGTCTTCACTTACGTTCAAAGTAATGCAACTGGTAAAGAACGTAATGGATTCTATAAAGACGGCTCTTATATTGATCATCAAGACGTCCCATACACTGGTGCTTATGGCGTTGTACTCTTAGAGGGGATTTCTCAAATGATGCCGATGATAAAAGAAACACCTTTTAAAGATAGTAATCAAAATGATACAACATTAAAGTCGTGGATTGATGAAGGATTTATGCCACTCATTTATAAAGGTGAAATGATGGATTTATCACGTGGTAGAGCCATTAGCCGTGAAAATGAAACGAGTCACTCAACATCTGCAACTGTAATGAAATCATTGTTGAGATTAAGTGATGCCATGGATGAGTCAACAAAAGCTAAATATAAGCAAATCGTTAAAACTTCTGTTAAATCTGATTCAAGTTATAAACAAAACGATTATTTAAGCTCTTATTCAGATATAAGCAAAATGAAGTCTTTAATTGAAGACAGCACTATTTCTACTAACGGTTTAACACAACAACTTAAAATATATAATGACATGAATCGTGTCACCTATCATAACAAAGACTTAGACTTTGCATTTGGCTTAAGTATGACGTCGAAAAACGTCGCACATTACGAAAGTATCAACGGAGAGAACTTAAAAGGTTGGCACACTGGTGCTGGAATGTCTTATTTATACAATAGCGATGTGAAACACTACCGTGATAACTTCTGGGCGACAGCTGATATGAAACGTTTAGCAGGTACTACAACTTTAGATAATGAAGAACCTAAAGAAAATAAGAACTCCGATAAAACTTTTGTAGGCGGAACAAAATTCGATGACCAACATGCTAGTATCGGAATGGATTTTGAAAATCAGGACAAAACTTTAACTGCCAAAAAATCATATTTCATATTAAACGATAAAATTGTCTTCTTAGGAACTGGCATTAAAAGTACTGATTCATCAAAGAATCCAGTGACAACGATTGAAAATCGCAAATCGAATGGGTATACGTTATTTACAGACGATAAACAAACAACCGCTTCAAATATTAATGATCAGGAAACCAATTCAGTC11111AGAGTCCACAGATACAAAAAAGAACATCGGTTATCATTTTTTAAACGAATCGAAAATAACTGTAAAAAAAGAAAGTCATACTGGTAAGTGGAGTGATATAAATAAAAGTCAAAAGTCAGATGACAAAACTGATGAGTATTATGAAGTAACTCAAAAGCATTCTAATACAGATGATAAATATGCATATGTCTTGTATCCAGGCTTATCTAAAGATAATTTTAAATCCAAAGCAAGCCAAGTAACTATCGTTAAACAAGATGATGACTTCCACATTGTGAAAGATAATGAATCGGTTTGGGCTGGTGTCAATTATAGTAATAGCACTCAAACTTTTGACATTAACAACACCAAGGTTGAGGTTAAAGCGAAAGGGATGTTCATTTTGAAAAACAAGGACGATAATACGTACGAATGCTCATTCTATAATCCTGAGTCTACGAATACGGCTTCAGACATAGAAAGTAAGATCAGTATGACGGGATACTCAATCACGAATAAAAACACAAGTACGTCCAACGAAAGTGGTGTGCATTTCGAGTTGACTAAATATGCTGCCGCGATGTCTGGAGCAGGTCCGTGGGCAGCCTGGCCATTCCTACTCTCACTGGCGCTCATGCTACTATGGCTGCTCTCATGA 30 Hyaluronidase with IgE-derived signalsequence (protein) MDWTWILFLVAAATRVHSGRDTNVQTPDYEKLRNTWLNVNYGYDQYDEKNDAMKKKFDATEKEAEKLLSSMKTESGRTYLWDSAKDLDNKSADMTRTYRNIEKIAEAMKHKDTKLNTPDNKNKVKDALEWLHKNAYGKEPVKKLEELKTNFSKSAPQKNTNLNWWDYEIGTPRALTNTLILLKEDFTDEEKKKYTAPIKTFAPKSDEILSSVGKAEPAKGGNLVDISKVKLLESIIEEDATMMKESIEAFNKVFTYVQSNATGKERNGFYKDGSYIDHQDVPYTGAYGVVLLEGISQMMPMIKETPFKDSNQNDTTLKSWIDEGFMPLIYKGEMMDLSRGRAISRENETSHSTSATVMKSLLRLSDAMDESTKAKYKQIVKTSVKSDSSYKQNDYLSSYSDISKMKSLIEDSTISTNGLTQQLKIYNDMNRVTYHNKDLDFAFGLSMTSKNVAHYESINGENLKGWHTGAGMSYLYNSDVKHYRDNFWATADMKRLAGTTTLDNEEPKENKNSDKTFVGGTKFDDQHASIGMDFENQDKTLTAKKSYFILNDKIVFLGTGIKSTDSSKNPVTTIENRKSNGYTLFTDDKQTTASNINDQETNSVFLESTDTKKNIGYHFLNESKITVKKESHTGKWSDINKSQKSDDKTDEYYEVTQKHSNTDDKYAYVLYPGLSKDNFKSKASQVTIVKQDDDFHIVKDNESVWAGVNYSNSTQTFDINNTKVEVKAKGMFILKNKDDNTYECSFYNPESTNTASDIESKISMTGYSITNKNTSTSNESGVHFELTKYAAAMSGAGPWAAWPFLLSLALMLLWLLS 31 IL-2 (mouse, DNA)AATTCTATGGCTCCGACTTCAAGTTCTACCAAGAAGACCCAGCTTCAATTAGAACATTTACTTCTAGATTTACAAATGATTCTGAATGGTATCAACAATTATAAGAATCCAAAGCTTACTCGTATGTTGACCTTTAAATTCTATATGCCTAAGAAGGCTACTGAATTAAAACACCTGCAGTGTTTAGAAGAAGAGCTCAAACCGTTAGAAGAAGTTCTGAATCTGGCTCAATCTAAAAACTTCCATTTACGTCCACGAGATCTTATCTCTAATATTAACGTAATCGTTTTGGAACTTAAAGGATCCGAAACTACCTTCATGTGTGAATATGCTGACGAAACCGCTACGATCGTAGAATTTCTTAATCGATGGATTACTTTCTGTCAATCTATTATCTCTACC TTAACTTGAGTCGACG 32 IL-2(human, DNA) ATGTACAGGATGCAACTCCTGTCTTGCATTGCACTAAGTCTTGCACTTGTCACAAACAGTGCACCTACTTCAAGTTCTACAAAGAAAACACAGCTACAACTGGAGCATTTACTGCTGGATTTACAGATGATTTTGAATGGAATTAATAATTACAAGAATCCCAAACTCACCAGGATGCTCACATTTAAGTTTTACATGCCCAAGAAGGCCACAGAACTGAAACATCTTCAGTGTCTAGAAGAAGAACTCAAACCTCTGGAGGAAGTGCTAAATTTAGCTCAAAGCAAAAACTTTCACTTAAGACCCAGGGACTTAATCAGCAATATCAACGTAATAGTTCTGGAACTAAAGGGATCTGAAACAACATTCATGTGTGAATATGCTGATGAGACAGCAACCATTGTAGAATTTCTGAACAGATGGATTACCTTTTGTCAAAGCAT CATCTCAACACTGACTTGA 33IL-2 (mouse, protein) MYSMQLASCVTLTLVLLVNSAPTSSSTSSSTAEAQQQQQQQQQQQQHLEQLLMDLQELLSRMENYRNLKLPRMLTFKFYLPKQATELKDLQCLEDELGPLRHVLDLTQSKSFQLEDAENFISNIRVTVVKLKGSDNTFECQFDDESATVVDFLRRWIAFCQSIISTSPQ 34 IL-2 (human, protein)MYRMQLLSCIALSLALVTNSAPTSSSTKKTQLQLEHLLLDLQMILNGINNYKNPKLTRMLTFKFYMPKKATELKHLQCLEEELKPLEEVLNLAQSKNFHLRPRDLISNINVIVLELKGSETTFMCEYADETATIVEFLNR WITFCQSIISTLT 35 loxPATAACTTCGTATAGCATACATTATACGAAGTTAT 36 dnIRF7 (DNA)ATGCCAGGGCTCCCTGCTGGGGAGCTGTACGGGTGGGCAGTAGAGACGACCCCCAGCCCCGGGCCCCAGCCCGCGGCACTAACGACAGGCGAGGCCGCGGCCCCAGAGTCCCCGCACCAGGCAGAGCCGTACCTGTCACCCTCCCCAAGCGCCTGCACCGCGGTGCAAGAGCCCAGCCCAGGGGCGCTGGACGTGACCATCATGTACAAGGGCCGCACGGTGCTGCAGAAGGTGGTGGGACACCCGAGCTGCACGTTCCTATACGGCCCCCCAGACCCAGCTGTCCGGGCCACAGACCCCCAGCAGGTAGCATTCCCCAGCCCTGCCGAGCTACCGGACCAGAAGCAGCTGCGCTACACGGAGGAACTGCTGCGGCACGTGGCCCCTGGGTTGCACCTGGAGCTTCGGGGGCCACAGCTGTGGGCCCGGCGCATGGGCAAGTGCAAGGTGTACTGGGAGGTGGGCGGACCCCCAGGCTCCGCCAGCCCCTCCACCCCAGCCTGCCTGCTGCCTCGGAACTGTGACACCCCCATCTTCGACTTCAGAGTCTTCTTCCAAGAGCTGGTGGAATTCCGGGCACGGCAGCGCCGTGGCTCCCCACGCTATACCATCTACCTGGGCTTCGGGCAGGACCTGTCAGCTGGGAGGCCCAAGGAGAAGAGCCTGGTCCTGGTGAAGCTGGAACCCTGGCTGTGCCGAGTGCACCTAGAGGGCACGCAGCGTGAGGGTGTGTCTTCCCTGGATAGCAGCAGCCTCAGCCTCTGCCTGTCCAGCGCCAACAGCCTCTATGACGACATCGAGTGCTTCCTTATGGAGCTGGAGCAGCCCGCCTAG 37 dnIRF7 (polypeptide)MPGLPAGELYGWAVETTPSPGPQPAALTTGEAAAPESPHQAEPYLSPSPSACTAVQEPSPGALDVTIMYKGRTVLQKVVGHPSCTFLYGPPDPAVRATDPQQVAFPSPAELPDQKQLRYTEELLRHVAPGLHLELRGPQLWARRMGKCKVYWEVGGPPGSASPSTPACLLPRNCDTPIFDFRVFFQELVEFRARQRRGSPRYTIYLGFGQDLSAGRPKEKSLVLVKLEPWLCRVHLEGTQREGVSSLDSSSLSLCLSSANSLYDDIECFLMELEQPA 38 vIRF3 (DNA)ATGGCAGGCAGACGGCTTACATGGATCAGCGAGTTTATCGTAGGTGCCCTGGACTCTGATAAGTACCCCTTGGTAAAATGGCTTGATCGGTCAACGGGAACTTTTCTGGCTCCCGCTGCGAGAAATGACGTAATACCACTGGATTCCCTGCAGTTTTTCATAGATTTTAAGAGGGAGTGTTTGTCAAAGGGGCTCCACCCCCGAGATCTTTTGGGTAGTCCAATAACTGCGTTCGGTAAGATTTGTACAACTAGCCGACGGCTGAGACGATTGCCCGGTGAAGAGTACGAAGTTGTCCAAGGAATCAACTGCCGGCGGTGGCGGCTTCTCTGCGCCGAAGTGAAAGAATGCTGGTGGTGTGTACACGCGCGAACACATCTGCACTCCGGAAGCAGCCTTTGGGAAATTCTCTACCAGCATTCCGTAAGACTTGAAAAGCACCGACGAAGGCCCAGGCCCTTTGTAGGAGAGAACAGTGATTCTTCTGAGGAAGACCACCCTGCTTTCTGCGATGTGCCCGTAACACAAACGGGCGCGGAGAGCGAGGACAGCGGCGATGAAGGTCCTTCCACCAGACACAGCGCCTCAGGTGTCCAACCGGTAGACGATGCTAATGCCGACTCCCCTGGTTCTGGAGACGAAGGTCCCAGCACCCGCCATAGCGACAGTCAACCTCCTCCCGCCGATGAAACCACTGTCCACACAGACAATGTAGAGGACGATTTGACACTCCTTGATAAAGAGTCCGCGTGCGCATTGATGTATCACGTGGGGCAGGAGATGGACATGCTTATGCGAGCGATGTGCGATGAAGACTTGTTTGATTTGCTTGGGATCCCTGAGGATGTAATAGCCACAAGTCAGCCTGGTGGTGATACGGACGCCTCTGGCGTTGTTACGGAGGGTAGTATTGCTGCTAGCGCCGTGGGCGCAGGGGTTGAAGATGTCTACTTGGCAGGAGCCCTCGAAGCACAGAATGTCGCAGGGGAGTATGTGCTTGAGATCTCTGATGAGGAAGTAGACGATGGCGCTGGACTCCCTCCCGCCTCAAGGCGGAGACCCGTTGTTGGAGAGTTCTTGTGGGACGACGGTCCTAGGCGCCACGAAAGGCCAACGACCCGCAGAATTAGGCACAGGAAACTCAGGTCTGCGTACTACAGAGTAGCACGGCCCCCAGTGATGATCACGGACAGGCTGGGCGTTGAGGTTTTTTACTTCGGAAGGCCGGCTATGAGCCTTGAAGTGGAACGAAAAGTATTCATCTTGTGTAGCCAGAATCCGCTGGCAGACATCAGTCACTCCTGCCTCCATTCACGAAAAGGGCTTCGAGTCCTGCTGCCAAAACCGGACGACAATAATACTGGTCCGGGAGATGTTAACCTCCTCGCAGCGGTGTTGAGATCTTTTGCATCAGGCTTGGTGATAGTCTCACTCCGAAGCGGAATCTACGTGAAGAACCTCTGCAAGAGCACCGTCCTGTATCACGGAAACAACCCCCCAAAAAAGTTTGGCGTTATATGCGGACTTTCATCCAGAGCAGTTCTTGACGTGTTTAATGTTGCCCAATACCGGATTCAGGGCCATGAACACATCAAAAAGACAACCGTCTTCATCGGGGGAGACCCGACTTCAGCGGAGCAATTTGATATGGTGCCACTCGTTATCAAGCTTCGGTTGA GATCAGTGACGTGCGACGATTAA 39vIRF3 (polypeptide) MAGRRLTWISEFIVGALDSDKYPLVKWLDRSTGTFLAPAARNDVIPLDSLQFFIDFKRECLSKGLHPRDLLGSPITAFGKICTTSRRLRRLPGEEYEVVQGINCRRWRLLCAEVKECWWCVHARTHLHSGSSLWEILYQHSVRLEKHRRRPRPFVGENSDSSEEDHPAFCDVPVTQTGAESEDSGDEGPSTRHSASGVQPVDDANADSPGSGDEGPSTRHSDSQPPPADETTVHTDNVEDDLTLLDKESACALMYHVGQEMDMLMRAMCDEDLFDLLGIPEDVIATSQPGGDTDASGVVTEGSIAASAVGAGVEDVYLAGALEAQNVAGEYVLEISDEEVDDGAGLPPASRRRPVVGEFLWDDGPRRHERPTTRRIRHRKLRSAYYRVARPPVMITDRLGVEVFYFGRPAMSLEVERKVFILCSQNPLADISHSCLHSRKGLRVLLPKPDDNNTGPGDVNLLAAVLRSFASGLVIVSLRSGIYVKNLCKSTVLYHGNNPPKKFGVICGLSSRAVLDVFNVAQYRIQGHEHIKKTTVFIGGDPTSAEQFDMV PLVIKLRLRSVTCDD

We claim:
 1. A composition, wherein the composition comprises: an oncolytic virus, wherein the oncolytic virus comprises a genome modification, wherein the genome modification comprises an exogenous nucleic acid encoding for a membrane associated extracellular matrix (ECM) degrading enzyme comprising: a bacterial hyaluronidase enzyme or a functional variant thereof, wherein the bacterial hyaluronidase enzyme is soluble in its naturally occurring form; and an N-terminal secretory signal sequence; and a signal sequence for membrane association.
 2. The composition of claim 1, wherein the N-terminal secretory signal sequence comprises an IgE-derived signal sequence.
 3. The composition of claim 2, wherein the IgE-derived signal sequence is SEQ ID NO:
 7. 4. The composition of claim 1, wherein the bacterial hyaluronidase enzyme is from Staphylococcus aureus.
 5. The composition of claim 4, wherein the bacterial hyaluronidase enzyme is HysA.
 6. The composition of claim 5, wherein the bacterial hyaluronidase enzyme comprises an amino acid sequence having at least 95% sequence identity to SEQ ID NO:
 30. 7. The composition of claim 5, wherein the bacterial hyaluronidase enzyme comprises an amino acid sequence of SEQ ID NO:
 30. 8. The composition of claim 1, wherein the oncolytic virus comprises a poxvirus, an adeno associated virus, an adenovirus, Newcastle disease virus (NDV), Reovirus (RV), mengovirus, Myxoma virus (MYXV), Measles virus (MV), Herpes Simplex virus (HSV), Vaccinia virus (VV), Vesicular Stomatitis virus (VSV), and Polio virus (PV).
 9. The composition of claim 8, wherein the poxvirus comprises a betaentomopoxvirus, a yatapoxvirus, a cervidpoxvirus, a gammaentomopoxvirus, a leporipoxvirus, a suipoxvirus, a molluscipoxvirus, a crocodylidpoxvirus, an alphaentomopoxvirus, a capripoxvirus, an avipoxvirus, or a parapoxvirus.
 10. The composition of claim 1, wherein the oncolytic virus is a vaccinia virus.
 11. The composition of claim 1, wherein the genome modification reduces an immune response targeting a virus-infected tumor cell and increases an immune response targeting cells surrounding the virus-infected tumor cell.
 12. The composition of claim 1, wherein the genome modification comprises mutation or a complete or a partial deletion of a viral gene comprising at least one of: A52R, B15R, K7R, A46R, N1L, E3L, K1L, M2L, C16, N2R, B8R, B18R, or VH1 of a vaccinia virus or a functional domain or fragment or variant thereof, or any combinations thereof.
 13. The composition of claim 12, further comprising a deletion of a thymidine kinase gene.
 14. The composition of claim 1, further comprising a deletion of a thymidine kinase gene.
 15. The composition of claim 1, wherein the oncolytic virus is a vaccinia virus, and the vaccinia virus is a Western Reserve strain Vaccinia virus (ATCC VR-1354), a Copenhagen strain, an IHD strain, a Wyeth strain (ATCC VR-325), a NYCBOH strain, a Tian Tan strain, a Lister strain, an Ankara strain (ATCC VR-1508 or ATTC VR1566), a USSR strain, or an ACAM2000 strain.
 16. A method of treating cancer, comprising administering to a subject having cancer the oncolytic virus of claim
 1. 17. The method of claim 16, wherein the administration is intratumoral, intravenous, parenteral, intradermal, intramuscular, transdermal, rectal, intraurethral, intravaginal, intranasal, intrathecal, intraperitoneal, intradental, subcutaneous, percutaneous, intratracheal, intraarterial, intravesical, inhalation, or oral.
 18. The method of claim 16, wherein the administration is intratumoral.
 19. The method of claim 16, wherein the administration is intravenous.
 20. The method of claim 16, wherein the cancer is a solid cancer or a blood cancer. 